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6-Chloro-N-(4-methoxy-benzyl)-nicotinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

805303-96-2

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805303-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 805303-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,5,3,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 805303-96:
(8*8)+(7*0)+(6*5)+(5*3)+(4*0)+(3*3)+(2*9)+(1*6)=142
142 % 10 = 2
So 805303-96-2 is a valid CAS Registry Number.

805303-96-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-N-[(4-methoxyphenyl)methyl]pyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 6-chloro-N-(4-methoxy-benzyl)-nicotinamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:805303-96-2 SDS

805303-96-2Relevant academic research and scientific papers

Latent Bronsted Base Solvent-Assisted Amide Formation from Amines and Acid Chlorides

Otsuka, Rikuto,Maruhashi, Kazuo,Ohwada, Tomohiko

supporting information, p. 2041 - 2057 (2018/05/04)

Weakly basic amines, including even neutral amines such as nitroaniline and aminocarboxylic acids, react with acid chlorides very efficiently in N, N -dimethylacetamide (DMAC), without addition of a base, to give the corresponding amides in high yields. The role of DMAC and related solvents as latent Bronsted bases was studied in these amidation reactions. Less basic amines, such as aromatic amines, reacted with benzoyl chloride faster than more basic aliphatic amines.

SAR based design of nicotinamides as a novel class of androgen receptor antagonists for prostate cancer

Yang, Su Hui,Song, Chin-Hee,Van, Hue Thi My,Park, Eunsook,Khadka, Daulat Bikram,Gong, Eun-Yeung,Lee, Keesook,Cho, Won-Jea

, p. 3414 - 3418 (2013/06/05)

Molecular knowledge of pure antagonism and systematic SAR study offered a direction for structural optimization of DIMN to provide nicotinamides as a novel series of AR antagonists. Nicotinamides with extended linear scaffold bearing sterically bulky alkoxy groups on isoquinoline end were synthesized for H12 displacement. AR binding affinity and molecular basis of antiandrogenic effect establish the optimized derivatives, 7au and 7bb, as promising candidates of second generation AR antagonists for advanced prostate cancer.

P-38 kinase inhibitors

-

Page/Page column 26, (2008/06/13)

Compounds and compositions for modulating the activity of p38 kinases are provided, including p38α and p38β kinase. Methods for treating, preventing or ameliorating one or more symptoms of a p38 kinase mediated disease or disorder are also provided.

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