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51071-56-8

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51071-56-8 Usage

Chemical Composition

Amino group: A functional group consisting of a nitrogen atom attached by single bonds to hydrogen atoms, alkyl groups, aryl groups, or a combination of these three kinds of atoms. It is a basic group due to the lone pair of electrons on the nitrogen atom.
Benzyl group: An aryl group derived from benzene by removing one hydrogen, resulting in the structure -C6H5CH2-. This group adds both hydrophobic (lipophilic) properties and steric bulk to the molecule.
Pyridine ring: A heterocyclic aromatic organic compound with the formula C5H5N. It is a basic, six-membered ring structure with one nitrogen atom. Pyridine rings are known for their presence in many biologically active compounds.
Carboxamide group: An organic functional group with the formula CONH2. This group is derived from carboxylic acids (RCOOH) by replacing the hydroxyl group (-OH) with an amine group (-NH2). It imparts polar characteristics to the molecule, increasing its solubility in water.
Hydrochloride salt: Formed by the addition of hydrochloric acid to an amine. Hydrochloride salts are commonly used to make organic compounds more water-soluble, which is beneficial for drug formulation and bioavailability.

Biological Activity

Potential anti-tuberculosis agent: This compound has been identified as having promising activity against *Mycobacterium tuberculosis*, the bacterium responsible for tuberculosis (TB). Its structure allows it to interact with bacterial components, potentially inhibiting the bacterium's growth or survival.
Drug candidate for the treatment of tuberculosis: Due to its anti-tuberculosis activity, this compound is being researched as a possible therapeutic for TB treatment. Its effectiveness, safety, and pharmacokinetics are likely under investigation in preclinical and possibly early clinical studies.

Therapeutic Applications

Treatment of tuberculosis: Given its activity against *Mycobacterium tuberculosis*, 2-amino-N-benzylpyridine-3-carboxamide hydrochloride holds promise for development into a medication for TB, a global health concern with a need for new treatments due to rising drug resistance.

This detailed breakdown covers the specific content and properties of 2-amino-N-benzylpyridine-3-carboxamide hydrochloride, highlighting its structure, biological activity, and potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 51071-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,7 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51071-56:
(7*5)+(6*1)+(5*0)+(4*7)+(3*1)+(2*5)+(1*6)=88
88 % 10 = 8
So 51071-56-8 is a valid CAS Registry Number.

51071-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-N-benzylpyridine-3-carboxamide,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-amino-N-benzylpyridine-3-carboxamide hydrochloride

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:51071-56-8 SDS

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