Tag: M.W=100-150

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. Recommanded Product: (4-Chlorophenyl)methanamine.

Sun, Binshu;Zheng, Jianhong;Yin, Dewu;Jin, Huile;Wang, Xin;Xu, Quanlong;Liu, Aili;Wang, Shun research published 《 Dual cocatalyst modified CdS achieving enhanced photocatalytic H₂ generation and benzylamine oxidation performance》, the research content is summarized as follows. Cocatalyst can greatly facilitate the charge separation efficiency and decrease the activation barrier of a specific reaction, thus contributing the improved photocatalytic performance. Herein, PdS/CdS/MoS₂ was synthesized via a facile microwave-assisted approach. Owing to the coexistence of PdS and MoS₂, resp. serving as oxidation and reduction cocatalyst, PdS/CdS/MoS₂ displayed enhanced photocatalytic performance in both hydrogen production (6610 μmol·g^-1·h^-1) and benzylamine oxidation (87% conversion) in comparison with the individual and binary composite counterparts. The improved photocatalytic activity was mainly attributed to the high charge separation efficiency and lowed activation barrier. Furthermore, the introduction of PdS can timely extract photogenerated holes from CdS, which effectively inhibits the photo-corrosion of CdS, endowing it with high stability. This work paves the way for developing efficient chalcogenide photocatalysts.

Recommanded Product: (4-Chlorophenyl)methanamine, 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. COA of Formula: C7H8ClN.

Sun, Jie;Nie, Qigui;Fang, Xianfu;He, Zhiwei;Zhang, Gong;Li, Yangfeng;Li, Yizhou research published 《 Vinyl azide as a synthon for DNA-compatible divergent transformations into N-heterocycles》, the research content is summarized as follows. Inspired by diversity-oriented synthesis, a series of DNA-compatible transformations utilizing on-DNA vinyl azide as a synthon to forge divergent N-heterocyclic scaffolds was developed. Polysubstituted imidazoles and isoquinolines were efficiently obtained with moderate-to-excellent conversions. Besides, the “one-pot” strategy to prepare inhouse on-DNA vinyl azides afforded synthons readily. Results from substrate scope exploration and enzymic ligation further demonstrate the feasibility of these N-heterocycle syntheses in DNA-encoded chem. library construction.

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., COA of Formula: C7H8ClN

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

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 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 names and applications. Application of C7H8ClN.

Sharma, Charu;Srivastava, Avinash K.;Sharma, Deepak;Joshi, Raj K. research published 《 Iron- and copper-based bifunctional catalysts for the base- and solvent-free C-N coupling of amines and aryl/benzyl chlorides under aerobic conditions》, the research content is summarized as follows. The iron chalcogenide carbonyl cluster Fe₃Se₂(CO)₉ and Cu(OAc)₂ were found to be outstanding bimetallic catalysts for the C-N coupling reaction of amines and aryl chlorides. The reaction proceeded under base- and solvent-free conditions at 100°C to produce excellent transformations of N-arylated products in just 4 h. The method worked equally well for all the possible variants of amines, including aliphatic, aromatic and benzylic amine. The present C-N coupling method was highly economical, strongly feasible and showed excellent competence with electron-withdrawing and base-sensitive functionalities. Moreover, it was the first report in which a zero-valent iron complex was explored for C-N coupling reaction.

Application of C7H8ClN, 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. SDS of cas: 104-86-9.

Si, Tengda;Kim, Hun Young;Oh, Kyungsoo research published 《 One-Pot Direct Oxidation of Primary Amines to Carboxylic Acids through Tandem ortho-Naphthoquinone-Catalyzed and TBHP-Promoted Oxidation Sequence》, the research content is summarized as follows. Biomimetic oxidation procedure for primary amines ArCH₂NH₂ (Ar = Ph, naphthalen-1-yl, thiophen-2-yl, etc.) to carboxylic acids ArCOOH has been developed where the copper-containing amine oxidase (CuAO)-like o-NQ-catalyzed aerobic oxidation was combined with the aldehydes RCHO (R = n-Pr, pyridin-3-yl, 4-chlorophenyl, etc.) dehydrogenase (ALDH)-like TBHP-mediated [(4-chlorophenyl)methyl][(4-chlorophenyl)methylidene]amine oxidation protocol. Notably, the current tandem oxidation strategy provides a new mechanistic insight into the imine intermediate and the seemingly simple TBHP-mediated oxidation pathways of imines. The developed metal-free amine oxidation protocol allows the use of mol. oxygen and TBHP, safe forms of oxidant that may appeal to the industrial application.

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., SDS of cas: 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). 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Quality Control of 104-86-9.

Sarkar, Prabhat;Mukhopadhyay, Chhanda research published 《 Base-Free I₂ -Catalyzed Robust Synthesis of Multi-Functionalized Aniline Scaffolds through Mild and Operationally Simple One-Pot Domino Protocol》, the research content is summarized as follows. A proficient, simple and feasible synthetic protocol was developed for the synthesis of polysubstituted 2,6-dicyanoaniline derivatives by one-pot domino approach towards the reaction between phenylethylidine malononitriles and benzyl amines as starting components catalyzed by I₂ at room temperature in MeCN:H₂O (5 : 1) solvent mixture Moreover, the choice of readily available starting materials having broad substrate scope under mild and operationally simple reaction conditions are the prominent advantages of this strategy.

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., Quality Control of 104-86-9

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

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 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 names and applications. HPLC of Formula: 104-86-9.

Satish, Sohal;Chitral, Rohan;Kori, Amitkumar;Sharma, Basantkumar;Puttur, Jayashree;Khan, Afreen A.;Desle, Deepali;Raikuvar, Kavita;Korkegian, Aaron;Martis, Elvis A. F.;Iyer, Krishna R.;Coutinho, Evans C.;Parish, Tanya;Nandan, Santosh research published 《 Design, synthesis and SAR of antitubercular benzylpiperazine ureas》, the research content is summarized as follows. N-furfuryl piperazine ureas disclosed by scientists at GSK Tres Cantos were chosen as antimycobacterial hits from a phenotypic whole-cell screen. Bioisosteric replacement of the furan ring in the GSK Tres Cantos mols. with a Ph ring led to mol. I with an MIC of 1μM against Mtb H37Rv, low cellular toxicity (HepG2 IC₅₀ ∼ 80μM), good DMPK properties and specificity for Mtb. With the aim of delineating the SAR associated with compound I, fifty-five analogs were synthesized and screened against Mtb. The SAR suggested that the piperazine ring, benzyl urea and piperonyl moieties were essential signatures of this series. Active compounds in this series were metabolically stable, have low cellular toxicity and were valuable leads for optimization. Mol. docking suggests these mols. occupy the Q0 site of QcrB like Q203.

HPLC of Formula: 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

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. Name: (4-Chlorophenyl)methanamine.

Seefeldt, Paul;Dasi, Rajesh;Villinger, Alexander;Brasholz, Malte research published 《 Photoredox-Induced Deaminative Radical-Cationic Three-Component Couplings with N-Alkylpyridinium Salts and Alkenes》, the research content is summarized as follows. N-Benzyl- and N-2°-alkylpyridinium salts were engaged in visible-light-driven, photoredox-induced radical-cationic three-component couplings with N-methylmaleimide and acrylonitrile as radical acceptors, in combination with 1,1-diarylethylenes as donor alkenes. These multicomponent coupling reactions could be achieved under mild conditions, with high efficiency, and to furnish diverse 3,4-disubstituted pyrrolidin-2,5-dione products with high stereoselectivity. In addition, 2,3-diaryl-1,3-butadienes could be utilized as alternative donor alkene components, to furnish diastereomerically pure 1,2,3-trisubstituted 1,3-butadienes as the coupling products.

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., Name: (4-Chlorophenyl)methanamine

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. COA of Formula: C7H8ClN.

Ranjan, Archana;Varma, Ajit;Kumari, Sangeeta;Joshi, Raj K. research published 《 Cu/Mn-Catalyzed C-N Cross-Coupling Reaction of Aryl Chlorides and Amines Promoted by a Polyamidoamine Dendrimer》, the research content is summarized as follows. A bimetallic catalytic combination of Mn(OAc)₂and Cu(OAc) ₂ was found to be significantly effective for the Buchwald-type C-N cross-coupling of aryl chlorides and amines. The reaction was markedly affected by the presence of a poly(amidoamine) dendrimer as a promoter that also possesses the advantages of being stable, nontoxic, biocompatible, nonimmunogenic, and acting as a soluble support for the transition-metal complex. Although, manganese was cheap and environmentally benign, it has not been fully exploited, due to its low intrinsic catalytic activity. Here, the catalytic potential of manganese was drastically increased by the presence of another metal salt, Cu(OAc)₂. In the bimetallic composition, Mn significantly influenced the activity and selectivity, and played a vital role in catalysis. A novel, green, and economical procedure for Buchwald-type C-N cross-coupling of aryl chlorides and amines was developed . This coupling method works under aerobic and solvent-free conditions and gives excellent yields of value-added N-arylated or N-alkylated products.

COA of Formula: C7H8ClN, 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

Chloride substituents modify the physical properties of organic compounds in several ways. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. COA of Formula: C7H8ClN.

Peng, Lingteng;Hu, Zhifang;Zhao, Yanting;Peng, Lifen;Xu, Zhi;Yin, Shuang-Feng;Tang, Zilong;Qiu, Renhua;Kambe, Nobuaki research published 《 One-pot synthesis of phosphorylnaphth[2,1-d]oxazoles and products as P,N-ligands in C-N and C-C formation》, the research content is summarized as follows. Phosphinylnaphtho[2,1-d]oxazoles were synthesized successfully through one-pot phosphonation of naphthoquinone with diaryl(alkyl)phosphine oxides and Cu-catalyzed oxidative condensation with imines, followed by methylation and reduction Upon applying 4-phosphinylnaphtho[2,1-d]oxazole as a P,N-chelating ligand, Pd-catalyzed C-N formation of amines or nitrobenzene as well as Ni-catalyzed C-C formation and the synthesis of quinoline proceeded successfully. The reaction was facilely scaled up to give a N-benzylaniline in a gram scale synthesis. This research provided a facile and convenient protocol to synthesize phosphinylnaphtho[2,1-d]oxazoles, which could be applied as an efficient P,N-ligand in transition-metal-catalyzed C-N and C-C formation to produce the desired products in high yields with wide functional group tolerance under small catalyst loading, solvent-free conditions in many reactions.

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., COA of Formula: C7H8ClN

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). 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Safety of (4-Chlorophenyl)methanamine.

Peng, Ting;He, Yujiao;Wang, Tao;Yu, Jialing;Ma, Xiaofang;Zhou, Zongyuan;Sheng, Yuwen;Li, Lingyu;Peng, Huipan;Li, Sheng;Zou, Jiawei;Yuan, Yi;Zhao, Yongyun;Shi, Hailong;Li, Fu;Liu, Wanli;Hu, Kaifeng;Lu, Xiaoxia;Zhang, Guolin;Wang, Fei research published 《 Discovery of a Novel Small-Molecule Inhibitor Disrupting TRBP-Dicer Interaction against Hepatocellular Carcinoma via the Modulation of microRNA Biogenesis》, the research content is summarized as follows. MicroRNAs (miRNAs) are key players in human hepatocellular carcinoma (HCC) tumorigenesis. Therefore, small mols. targeting components of miRNA biogenesis may provide new therapeutic means for HCC treatment. By a high-throughput screening and structural simplification, we identified a small mol., CIB-3b (I), which suppresses the growth and metastasis of HCC in vitro and in vivo by modulating expression profiles of miRNAome and proteome in HCC cells. Mechanistically, CIB-3b phys. binds to transactivation response (TAR) RNA-binding protein 2 (TRBP) and disrupts the TRBP-Dicer interaction, thereby altering the activity of Dicer and mature miRNA production Structure-activity relationship study via the synthesis of 45 CIB-3b derivatives showed that some compounds exhibited a similar inhibitory effect on miRNA biogenesis to CIB-3b. These results support TRBP as a potential therapeutic target in HCC and warrant further development of CIB-3b along with its analogs as a novel therapeutic strategy for the treatment of HCC.

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., Safety of (4-Chlorophenyl)methanamine

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