Month: September 2022

Chlorinated organic compounds are found in nearly every class of biomolecules. 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Recommanded Product: (2-Chlorophenyl)boronic acid.

Hager, Joanna;Kang, Seongsoo;Chmielewski, Piotr J.;Lis, Tadeusz;Kim, Dongho;Stepien, Marcin research published 《 Acenaphthylene-fused ullazines: fluorescent π-extended monopyrroles with tunable electronic gaps》, the research content is summarized as follows. π-Extended dibenzoullazines, e.g., I (R = 2,6-idisopropylphenyl, 2,9-di-tert-Bu, etc.) containing an acenaphthylene subunit were designed and synthesized. Two different synthetic strategies were employed: route A, based on Pd-catalyzed cyclodehydrohalogenation of α,α-disubstituted N-arylpyrroles, and route B, using a dipolar 1,3-cycloaddition reaction of azomethine ylides (PAMYs) to functionalized acenaphthylenes. Mols. of the resulting ullazines were almost flat, leading to strong π-π interactions in the solid state. The new ullazines were highly fluorescent (with a quantum yield of up to 0.89 for the naphthalimide-fused system), and showed moderate solvatochromism with no fluorescence quenching in polar solvents. Stepwise two-electron oxidation of the ullazines was possible, yielding reversibly the corresponding ullazine radical cations and dications. Edge expansion of the ullazine core with methylene bridges was addnl. shown to produce an ullazine analog containing two seven-membered rings in its structure, which was characterized by axial chirality and could be resolved into enantiomers.

3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., Recommanded Product: (2-Chlorophenyl)boronic acid

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Quality Control of 3900-89-8.

Guo, Yuying;Chen, Jiabao;Ren, Dan;Du, Bo;Wu, Lei;Zhang, Yuanyuan;Wang, Zhouyu;Qian, Shan research published 《 Synthesis of osthol-based botanical fungicides and their antifungal application in crop protection》, the research content is summarized as follows. Plant pathogenic fungi decrease the quality and productivity of plant production The botanical fungicides have better biocompatibility and rapid biodegradation, little or no cross resistance, and the structural diversity, and thus are beneficial to deal with plant fungal diseases. Osthole has been widely used as the com. botanical fungicide against powdery mildew in China. In this article, a series of osthole derivatives were synthesized, which resp. contain different substituents on the benzene ring, at the C8-position and pyrone ring. All the target compounds were evaluated in vitro for their antifungal activity against resistant phytopathogenic fungi. Colletotrichum fragariae, Strawberry Botrytis cinerea, Kiwifruit Botrytis cinerea, Kiwifruit brown Rots, which are common in fruit fungal diseases. The compound 7-hydroxy-8-methyl-4-(trifuoromethyl)-2H-chromen-2-one (I) was identified as the most promising candidate with the EC₅₀ values at 38.7μg/mL against Colletotrichum Fragariae, 14.5μg/mL against Strawberry Botrytis Cinerea and 24.3μg/mL against Kiwifruit Botrytis Cinerea, resp., whereas the antifungal activity against resistant phytopathogenic fungi. of osthole is too low to be used (EC₅₀ > 400 ppm). The results of mycelial relative conductivity determination, PI uptake and fluorescence spectroscopy indicated that the cell membrane of fungi is the key action site of I. Besides, I has the potent inhibitory activity against both of plant and human pathogenic bacteria. Our studies showed that C₄ was worthy for further attention as a promising botanical fungicide candidate in crop protection.

3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., Quality Control of 3900-89-8

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chlorinated organic compounds are found in nearly every class of biomolecules. 2905-24-0, formula is C6H4BrClO2S, Name is 3-Bromobenzenesulfonyl chloride. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Name: 3-Bromobenzenesulfonyl chloride.

Guo, Sheng-Qiang;Yang, Hui-Qing;Jiang, Yu-Zhen;Wang, Ai-Lian;Xu, Guo-Qiang;Luo, Yong-Chun;Chen, Zhao-Xu;Zheng, Haixue;Xu, Peng-Fei research published 《 Organophotoredox catalytic four-component radical-polar crossover cascade reactions for the stereoselective synthesis of β-amido sulfones》, the research content is summarized as follows. Herein, a green and reliable strategy for the diastereoselective synthesis of β-amido sulfones R¹S(O)₂CH(R²)CH(Ar)NHC(O)R³ (R¹ = Me, 4-methylphenyl, naphth-2-yl, etc.; R² = H, Me, Et, Pr, isopropyl; Ar = Ph, 3,4-dichlorophenyl, naphth-2-yl, etc.; R³ = Me, cyclopopyl, Ph, etc.) and I through organophotoredox catalytic four-component radical-polar crossover cascade reactions was reported. This transformation features excellent atom-, step-, and redox economy and diastereoselectivity. Moreover, DFT calculation studies were performed to provide some insights into the origin of diastereoselectivity.

2905-24-0, 3-Bromobenzenesulfonyl chloride is an aryl sulfonyl chloride derivative. It participates in the synthesis of N-sulfonylanthranilic acid derivatives and potent P1′ benzenesulfonyl azacyclic urea human immunodeficiency virus (HIV) protease inhibitors.
3-Bromobenzenesulfonyl chloride is a molecule that can be used to inhibit the uptake of 3-bromobenzoate. The inhibition of uptake is due to the desymmetrization of the unsymmetrical, 3-bromobenzoate. This reaction leads to an increase in the concentration of 3-bromobenzoate. Inhibition studies have shown that 3-bromobenzenesulfonyl chloride has an inhibitory effect on cancer cells and apoptosis pathway. The structural studies have shown that this drug is synthetic and biphenyl can be synthesized from it. T-cell lymphomas have been shown to be inhibited by this drug and heart disease has also been inhibited., Name: 3-Bromobenzenesulfonyl chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 2905-24-0, formula is C6H4BrClO2S, Name is 3-Bromobenzenesulfonyl chloride. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Electric Literature of 2905-24-0.

Guo, Sheng-Qiang;Yang, Hui-Qing;Wang, Ai-Lian;Jiang, Yu-Zhen;Xu, Guo-Qiang;Luo, Yong-Chun;Chen, Zhao-Xu;Xu, Peng-Fei research published 《 Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions》, the research content is summarized as follows. A green and practical divergent Ritter-type amination via a photoredox catalytic four-component radical-polar crossover process was developed. This versatile protocol presents a modular and powerful strategy to access functionalized β-sulfonyl imides and imines under mild conditions from readily available and stable substrates with high atom-, step- and redox economy. Authors manipulated carboxylic acids and benzotriazoles to precisely attack the nitrilium ion instead of the carbocation, thus preventing many complicated side reactions of the photocatalytic reactions. Furthermore, the synthetic utility of this divergent Ritter reaction is further demonstrated by the late-stage modification of pharmaceutical and natural product derivatives

Electric Literature of 2905-24-0, 3-Bromobenzenesulfonyl chloride is an aryl sulfonyl chloride derivative. It participates in the synthesis of N-sulfonylanthranilic acid derivatives and potent P1′ benzenesulfonyl azacyclic urea human immunodeficiency virus (HIV) protease inhibitors.
3-Bromobenzenesulfonyl chloride is a molecule that can be used to inhibit the uptake of 3-bromobenzoate. The inhibition of uptake is due to the desymmetrization of the unsymmetrical, 3-bromobenzoate. This reaction leads to an increase in the concentration of 3-bromobenzoate. Inhibition studies have shown that 3-bromobenzenesulfonyl chloride has an inhibitory effect on cancer cells and apoptosis pathway. The structural studies have shown that this drug is synthetic and biphenyl can be synthesized from it. T-cell lymphomas have been shown to be inhibited by this drug and heart disease has also been inhibited., 2905-24-0.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 12112-67-3, formula is C16H24Cl2Ir2, Name is Chloro(1,5-cyclooctadiene)iridium(I) dimer. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Category: chlorides-buliding-blocks.

Guo, Panchi;Zhan, Miao research published 《 Iridium-Catalyzed Enantioconvergent Allylation of a Boron-Stabilized Organozinc Reagent》, the research content is summarized as follows. An Ir-catalyzed enantioconvergent coupling of the versatile B-stabilized organozinc reagent BpinCH₂ZnI with a racemic branched allylic carbonate was developed here, which differs from the authors’ previous work by using 1,1-bisborylmethane through the kinetic resolution process. The reaction has a broad substrate scope, and various chiral homoallylic organoboronic esters could be obtained in good yields with excellent enantioselectivities. The synthetic practicability of the products was demonstrated by their conversion to other useful families of compounds

Category: chlorides-buliding-blocks, Bis(1,5-cyclooctadiene)diiridium(I) is a useful research compound. Its molecular formula is C16H24Cl2Ir2-2 and its molecular weight is 671.7 g/mol. The purity is usually 95%.
Bis(1,5-cyclooctadiene)diiridium(I) Dichloride is a catalyst used in the iridium-catalyzed asymmetry hydrogenation of unfunctionalized exocyclic double carbon bonds. Also, it is used to test new NeoPHOX ligands derived from serine or threonine.
Bis(1,5-cyclooctadiene)diiridium(I) dichloride is an acid that can be prepared using a preparative method. It is an organometallic compound that can be used in the cross-coupling of activated terminal alkynes with aryl halides. Bis(1,5-cyclooctadiene)diiridium(I) dichloride has been synthesized by reacting furfural with chloride and acetonitrile. The ligand used was 2,2′-bipyridine. The reaction time to produce bis(1,5-cyclooctadiene)diiridium(I) dichloride is approximately three hours.
, 12112-67-3.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chloride substituents modify the physical properties of organic compounds in several ways. 12112-67-3, formula is C16H24Cl2Ir2, Name is Chloro(1,5-cyclooctadiene)iridium(I) dimer. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Category: chlorides-buliding-blocks.

Guerra Faura, Gabriel;Nguyen, Tena;France, Stefan research published 《 Catalyst-Controlled Chemodivergent Reactions of 2-Pyrrolyl-α-diazo-α-ketoesters and Enol Ethers: Synthesis of 1,2-Dihydrofuran Acetals and Highly Substituted Indoles》, the research content is summarized as follows. A catalyst-controlled, chemodivergent reaction of pyrrolyl-α-diazo-α-ketoesters, e.g., I (R = H, Et, Ph, R¹ = Me, Bn, Ts), with enol ethers, e.g., 2-methoxypropene, dihydropyran, and (1-ethoxyvinyl)benzene, is reported. While Cu(II) catalysts selectively promoted a [3+2]-cycloaddition to provide pyrrolyl-substituted 2,3-dihydrofuran (DHF) acetals, e.g., II, dimeric Rh(II) catalysts afforded 6-hydroxyindole-7-carboxylates, e.g., III, via an unreported [4+2]-benzannulation. The choice of enol ether proved to be crucial in determining both regioselectivity and yield of the resp. products (up to 91% yield for Cu(II) and 82% for Rh(II) catalysis). Furthermore, the DHF acetals were shown to serve as precursors to 7-hydroxyindole-6-carboxylates (isomeric to the indoles formed from Rh) and highly substituted furans in the presence of Lewis acids. Thus, from a common pyrrolyl-α-diazo-α-ketoester, up to three unique heterocyclic scaffolds can be achieved based on catalyst selection.

Category: chlorides-buliding-blocks, Bis(1,5-cyclooctadiene)diiridium(I) is a useful research compound. Its molecular formula is C16H24Cl2Ir2-2 and its molecular weight is 671.7 g/mol. The purity is usually 95%.
Bis(1,5-cyclooctadiene)diiridium(I) Dichloride is a catalyst used in the iridium-catalyzed asymmetry hydrogenation of unfunctionalized exocyclic double carbon bonds. Also, it is used to test new NeoPHOX ligands derived from serine or threonine.
Bis(1,5-cyclooctadiene)diiridium(I) dichloride is an acid that can be prepared using a preparative method. It is an organometallic compound that can be used in the cross-coupling of activated terminal alkynes with aryl halides. Bis(1,5-cyclooctadiene)diiridium(I) dichloride has been synthesized by reacting furfural with chloride and acetonitrile. The ligand used was 2,2′-bipyridine. The reaction time to produce bis(1,5-cyclooctadiene)diiridium(I) dichloride is approximately three hours.
, 12112-67-3.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

The class of organic compounds having covalently a bonded chlorine atom is called organic chlorides. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Their wide structural variety and divergent chemical properties lead to a broad range of named reactions and applications. Quality Control of 104-86-9.

Guan, Dongliang;Rahman, Toufiqur Md;Gay, Elaine A.;Vasukuttan, Vineetha;Mathews, Kelly M.;Decker, Ann M.;Williams, Alexander H.;Zhan, Chang-Guo;Jin, Chunyang research published 《 Indole-Containing Amidinohydrazones as Nonpeptide, Dual RXFP3/4 Agonists: Synthesis, Structure-Activity Relationship, and Molecular Modeling Studies》, the research content is summarized as follows. Herein, the first structure-activity relationship studies of a series of novel nonpeptide amidinohydrazone-based agonists I [R¹ = H, 4-Me, 7-F, etc.; R² = H, Me; R³ = ; 4-ClC₆H₄, 3,4-di-ClC₆H₃, 2-thienyl, etc.; R⁴ = H, Me; n = 0,1,2,3], which were characterized by RXFP3 functional and radioligand binding assays was reported. Several potent and efficacious RXFP3 agonists compound I [R¹ = 5-CN-7-Me, R² = H, R³ = 4-CO₂MeC₆H₄, R⁴ = H, n = 2] were identified with EC₅₀ values <10 nM. These compounds also had high potency at RXFP4 but no agonist activity at RXFP1, demonstrating > 100-fold selectivity for RXFP3/4 over RXFP1. In vitro ADME and pharmacokinetic assessments revealed that the amidinohydrazone derivatives might have limited brain permeability.

Quality Control of 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chlorinated organic compounds are found in nearly every class of biomolecules. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Reference of 104-86-9.

Gu, Ai-Ling;Zhang, Ya-Xin;Wu, Zhi-Lei;Cui, Hui-Ya;Hu, Tian-Ding;Zhao, Bin research published 《 Highly Efficient Conversion of Propargylic Alcohols and Propargylic Amines with CO₂ Activated by Noble-Metal-Free Catalyst Cu₂O@ZIF-8》, the research content is summarized as follows. The cyclization reactions of propargylic alcs. and propargylic amines with CO₂ are important in industrial applications, but it was a great challenge that non-noble-metal catalysts catalyzed both reactions under mild conditions. Herein, the catalyst Cu₂O@ZIF-8 was prepared by encapsulating Cu₂O nanoparticles into robust ZIF-8, and it can effectively catalyze the cyclization of both propargylic alcs. and propargylic amines with CO₂ into valuable α-alkylidene cyclic carbonates and oxazolidinones with turnover numbers (TONs) of 12.1 and 19.6, which can be recycled at least five times. The mechanisms were further uncovered by NMR, FTIR, ¹³C isotope-labeling experiments and DFT calculations, in which Cu₂O and DBU can synergistically activate the C≃C bond and the hydroxy/amino group of substrates. Importantly, it is the first example of a noble-metal-free catalyst that can catalyze both propargylic alcs. and propargylic amines with CO₂ simultaneously.

Reference of 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 12112-67-3, formula is C16H24Cl2Ir2, Name is Chloro(1,5-cyclooctadiene)iridium(I) dimer. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Application In Synthesis of 12112-67-3.

Grimm, Alexandra B.;Wang, Kai;Rheingold, Arnold L.;Moore, Curtis E.;Szieberth, Denes;Nyulaszi, Laszlo;Protasiewicz, John D. research published 《 2-Aryl-1,3-Benzoxaphospholes as Unwilling Participants for Catalytic Suzuki-Miyaura CC Coupling Reactions》, the research content is summarized as follows. Under conditions typically effective to achieve a catalytic aryl-aryl bond during Pd Suzuki-Miyaura (SM) coupling reactions of ArB(OH)₂ and ArBr, reactions of p-tolylboronic acid and 2-(BrC₆H₄)-1,3-benzoxaphosphole (BrC₆H₄-BOP, 1) failed to provide the anticipated product of CC bond coupling, 2-(p-CH₃C₆H₄-C₆H₄)-1,3-benzoxaphosphole. An anal. of reaction mixtures by ¹H and ³¹P{¹H} NMR spectroscopic methods showed numerous broad resonances, suggesting the formation of labile metal complexes with 1. This possibility was confirmed by determinations of the solid-state structures of [(^tBu₃P)(Ph-BOP)M]₂ (M = Pt, 5; M = Pd, 6) from the reaction of Ph-BOP and [M(^tBu₃P)₂] (M = Pt, Pd). The structures of 5 and 6 are isomorphous and reveal unusual bridging μ₂-P-BOP bonding modes. Computational studies have explored the structures and relative energies and indicate that dimeric complexes of this form can dissociate easily. Surprisingly, even when P:C double bonds of Ar-BOPs are sheltered by coordination to W pentacarbonyl, the Ar-BOP units resist yielding products of CC coupling under similar SM conditions but instead yield unusual products whereby CsOH adds across the P:C bonds in [(CO)₅W{2-Ar-BOP}]. Computational studies are consistent with ready addition of hydroxide to the W-protected P:C bond.

Application In Synthesis of 12112-67-3, Bis(1,5-cyclooctadiene)diiridium(I) is a useful research compound. Its molecular formula is C16H24Cl2Ir2-2 and its molecular weight is 671.7 g/mol. The purity is usually 95%.
Bis(1,5-cyclooctadiene)diiridium(I) Dichloride is a catalyst used in the iridium-catalyzed asymmetry hydrogenation of unfunctionalized exocyclic double carbon bonds. Also, it is used to test new NeoPHOX ligands derived from serine or threonine.
Bis(1,5-cyclooctadiene)diiridium(I) dichloride is an acid that can be prepared using a preparative method. It is an organometallic compound that can be used in the cross-coupling of activated terminal alkynes with aryl halides. Bis(1,5-cyclooctadiene)diiridium(I) dichloride has been synthesized by reacting furfural with chloride and acetonitrile. The ligand used was 2,2′-bipyridine. The reaction time to produce bis(1,5-cyclooctadiene)diiridium(I) dichloride is approximately three hours.
, 12112-67-3.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 3900-89-8, formula is C6H6BClO2, Name is (2-Chlorophenyl)boronic acid. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Synthetic Route of 3900-89-8.

Grenz, David C.;Rose, Daniel;Wossner, Jan S.;Wilbuer, Jennifer;Adler, Florin;Hermann, Mathias;Chan, Chin-Yiu;Adachi, Chihaya;Esser, Birgit research published 《 Spiroconjugated Tetraaminospirenes as Donors in Color-Tunable Charge-Transfer Emitters with Donor-Acceptor Structure》, the research content is summarized as follows. Charge-transfer emitters are attractive due to their color tunability and potentially high photoluminescence quantum yields (PLQYs). Herein, the authors present tetraaminospirenes as donor moieties, which, in combination with a variety of acceptors, furnished 12 charge-transfer emitters with a range of emission colors and PLQYs of up to 99%. The spatial separation of their frontier MOs was obtained through careful structural design, and two donor-acceptor structures were confirmed by X-ray crystallog. A range of photophys. measurements supported by DFT calculations shed light on the optoelectronic properties of this new family of spiro-NN-donor-acceptor dyes.

3900-89-8, 2-Chlorophenylboronic acid is a useful research compound. Its molecular formula is C6H6BClO2 and its molecular weight is 156.38 g/mol. The purity is usually 95%.
2-Chlorophenylboronic acid used in the preparation of imidazo[1,2-a]pyridine amides which has tuberculostatic activity.
2-Chlorophenylboronic acid is a diphenyl ether that can be used as a building block for the synthesis of benzodiazepine receptor ligands. It has been shown to be an efficient nucleophile, leading to the formation of carbonyl groups in the presence of halides. 2-Chlorophenylboronic acid has also been shown to inhibit p38 kinase activity and may be useful for anticancer therapy., Synthetic Route of 3900-89-8

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics