Month: December 2022

Synthesis of some novel heterocyclic azo dyes for acridine derivatives and evaluation of their antibacterial activities was written by Shihab, Nezar L.;Intedhar, K. M.. And the article was included in Journal of Chemical and Pharmaceutical Research in 2013.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Five new azo dye containing acridine derivatives (e.g., I) were synthesized using different approaches depending on the position of the functional groups. The synthesis started with unsubstituted acridine that was converted by nitration and amination to 2,9-diaminoacridine which was subjected to diazotization with (2,4-dichloro-6-triazinyl)aniline DCTA. The structures of the newly synthesized compounds were characterized by NMR, Mass, FT-IR spectra data and elemental anal. All the synthesized compounds were screened for their antibacterial activities. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes was written by Wang, Guang-Zu;Jiang, Jian;Bu, Xiao-Song;Dai, Jian-Jun;Xu, Jun;Fu, Yao;Xu, Hua-Jian. And the article was included in Organic Letters in 2015.Related Products of 6294-17-3 The following contents are mentioned in the article:

The cross-coupling reaction of allyl boron ester with 1°/2°/3°-halogenated alkanes in the presence of copper has been developed for the first time, which provides a mild and efficient method for the construction of saturated C(sp³)-C(sp³) bonds. E.g., in presence of CuI and LiOCMe₃ in DMF, cross-coupling of allylboronic acid pinacol ester with 1-(4-bromobutyl)indole gave 87% I. This protocol shows excellent compatibility with the nonactivated primary, secondary, and even tertiary halogenated alkanes under mild conditions. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Related Products of 6294-17-3).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Related Products of 6294-17-3

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

Photoredox B-H functionalization to selective B-N(sp³) coupling of nido-carborane with primary and secondary amines was written by Huang, Ronghui;Zhao, Weijia;Xu, Shengwen;Xu, Jingkai;Li, Chunxiao;Lu, Changsheng;Yan, Hong. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2021.Category: chlorides-buliding-blocks The following contents are mentioned in the article:

Access to nido-carborane site-selective B-N(sp³) coupling by photoredox catalyzed B-H activation has been achieved for the first time, which leads to the synthesis of a series of nitrogen-containing nido-carboranes with moderate to good yields. This protocol is applicable to primary and secondary amines containing alkyl, or heteroaryl groups as well as sulfonamides. Furthermore, the open to air and metal-free conditions with excellent site-selectivity represent a significant improvement for B-H functionalization of nido-carboranes with organic functionalities. This study involved multiple reactions and reactants, such as Tetramethylammonium chloride (cas: 75-57-0Category: chlorides-buliding-blocks).

Tetramethylammonium chloride (cas: 75-57-0) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Category: chlorides-buliding-blocks

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

Iron-Catalyzed Borylation of Alkyl Electrophiles was written by Atack, Thomas C.;Lecker, Rachel M.;Cook, Silas P.. And the article was included in Journal of the American Chemical Society in 2014.Product Details of 6294-17-3 The following contents are mentioned in the article:

The use of low-cost iron(III) acetoacetate (Fe(acac)₃) and tetramethylethylenediamine (TMEDA) enables the direct cross-coupling of alkyl halides with bis(pinacolato)diboron. This approach allows for the borylation of activated or unactivated primary, secondary, and tertiary bromides. Moreover, even the borylation of benzylic or allylic chlorides, tosylates, and mesylates are possible. The reactions proceed under mild conditions at room temperature and show broad functional-group compatibility and “robustness” as measured by a modified Glorius robustness screen. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Product Details of 6294-17-3).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Product Details of 6294-17-3

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

Gold-Catalyzed Bicyclic Annulations of 2-Alkynylbenzaldehydes with Vinyldiazo Carbonyls that Serve as Five-atom Building Units was written by Raj, Antony Sekar Kulandai;Liu, Rai-Shung. And the article was included in Angewandte Chemie, International Edition in 2019.Synthetic Route of C15H9ClO The following contents are mentioned in the article:

In the presence of (PhO)₃PAuCl and AgOTf, α-diazo-β,γ-unsaturated ketones such as H₂C:CHC(:N₂)COPh underwent diastereoselective cyclization reactions with ortho-alkynylbenzaldehydes such as 2-(phenylethynyl)benzaldehyde to yield tetrahydrobenzindazoles such as I in which five atoms of the diazo compound are incorporated into the product. Mechanistic experiments provided evidence for a mechanism involving the initial [5+4]-cycloaddition of a benzopyrylium intermediate and a vinyldiazoketone followed by 6π-electrocyclization. This study involved multiple reactions and reactants, such as 5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3Synthetic Route of C15H9ClO).

5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Synthetic Route of C15H9ClO

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

Chemo-enzymatic approach to the synthesis of the antithrombotic clopidogrel was written by Ferraboschi, Patrizia;De Mieri, Maria;Galimberti, Fiorella. And the article was included in Tetrahedron: Asymmetry in 2010.Recommanded Product: 141109-14-0 The following contents are mentioned in the article:

The (S)-2-chlorophenylglycine moiety is well recognized in the structure of (S)-clopidogrel, a known antithrombotic drug. An enantiomerically pure chiral building block was prepared via an enzyme-catalyzed resolution of (RS)-N-Boc-2-chlorophenylglycine Me ester. The best results were obtained by means of an immobilized subtilisin, the cross-linked enzyme aggregate (Alcalase-CLEA). The high enantiomeric excess of the synthon obtained remained the same over the course of clopidogrel synthesis; the simplicity of the process makes this pathway suitable for large-scale preparation This study involved multiple reactions and reactants, such as (S)-Methyl 2-amino-2-(2-chlorophenyl)acetate (cas: 141109-14-0Recommanded Product: 141109-14-0).

(S)-Methyl 2-amino-2-(2-chlorophenyl)acetate (cas: 141109-14-0) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Recommanded Product: 141109-14-0

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

Synthesis and bioevaluation of hybrid 4-aminoquinoline triazines as a new class of antimalarial agents was written by Kumar, Ashok;Srivastava, Kumkum;Raja Kumar, S.;Puri, S. K.;Chauhan, Prem M. S.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2008.Related Products of 2272-40-4 The following contents are mentioned in the article:

The emergence and rapid spread of chloroquine resistant strains of Plasmodium falciparum has dramatically reduced the chemotherapeutic options. Towards this goal, a series of new class of hybrid 4-aminoquinoline triazines were synthesized and screened against CQ sensitive strain 3D7 of P. falciparum in an in vitro model. Compounds I and II exhibited more than 99% suppression on day 4 and on day 6 post treatment, compound II showed impressive 99.11% suppression against CQ resistant strain N-67 of P. yoelii in an in vivo assay. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Related Products of 2272-40-4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Related Products of 2272-40-4

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

Visible light-assisted Ni-/Ir-catalysed atom-economic synthesis of spiro[furan-3,1′-indene] derivatives was written by Gore, Babasaheb Sopan;Kuo, Chiao-Ying;Wang, Jeh-Jeng. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2022.Computed Properties of C15H9ClO The following contents are mentioned in the article:

An atom-economic, efficient, and highly convenient construction of spiro[furan-3,1′-indene] skeletons from isocyanides and 1,5-enynes by synergistic nickel- and iridium-photocatalysis is reported. Spirocyclization was developed under practical and mild conditions, which features excellent functional group tolerance, gram-scale synthesis and representative synthetic transformations for the obtained products and broad substrate scope. Primary mechanistic studies demonstrated that the reaction proceeds through energy-transfer-mediated excitation of intermediate catalytic species. This study involved multiple reactions and reactants, such as 5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3Computed Properties of C15H9ClO).

5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Computed Properties of C15H9ClO

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

Comparative studies of novel triazole derivative having chiral center and their antimicrobial activities was written by Mistry, Bhavnaben D.;Desai, Kishor R.;Intwala, Sanket M.. And the article was included in Pharma Chemica in 2013.Formula: C9H10ClNO2 The following contents are mentioned in the article:

The compounds 1,2,4-triazole-3-thiol derivatives (-) and (+)-I [R = H, 3-CH₃, 2-OH, 3,5-(NH₂)₂] have been synthesized by the reaction of 1,3,4-oxadiazole-2-thiol derivatives (-) and (+)-II with concentrate H₂SO₄, L-(+) tartaric acid, D-(-) tartaric acid, hydrazine hydrate, carbon disulfide and various aromatic amine resp.. The synthesized compounds have been screened for their antibacterial and antifungal activities against different microorganisms. This study involved multiple reactions and reactants, such as (S)-Methyl 2-amino-2-(2-chlorophenyl)acetate (cas: 141109-14-0Formula: C9H10ClNO2).

(S)-Methyl 2-amino-2-(2-chlorophenyl)acetate (cas: 141109-14-0) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Formula: C9H10ClNO2

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

Optimization of ADME Properties for Sulfonamides Leading to the Discovery of a T-Type Calcium Channel Blocker, ABT-639 was written by Zhang, Qingwei;Xia, Zhiren;Joshi, Shailen;Scott, Victoria E.;Jarvis, Michael F.. And the article was included in ACS Medicinal Chemistry Letters in 2015.Application In Synthesis of 2-Chloro-5-(chlorosulfonyl)-4-fluorobenzoyl chloride The following contents are mentioned in the article:

The discovery of a novel peripherally acting and selective Ca_v3.2 T-type calcium channel blocker, ABT-639 I, is described. HTS hits, which have poor metabolic stability, were optimized to obtain a lead, which has improved stability and oral bioavailability. Modification of the lead to further improve ADME properties led to the discovery of I. Following oral administration, I produces robust antinociceptive activity in exptl. pain models at doses that do not significantly alter psychomotor or hemodynamic function in the rat. This study involved multiple reactions and reactants, such as 2-Chloro-5-(chlorosulfonyl)-4-fluorobenzoyl chloride (cas: 866763-17-9Application In Synthesis of 2-Chloro-5-(chlorosulfonyl)-4-fluorobenzoyl chloride).

2-Chloro-5-(chlorosulfonyl)-4-fluorobenzoyl chloride (cas: 866763-17-9) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Application In Synthesis of 2-Chloro-5-(chlorosulfonyl)-4-fluorobenzoyl chloride

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