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127915-50-8

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127915-50-8 Usage

General Description

3-Pyridinecarboxylic acid, 4-amino-6-methyl-, also known as 4-amino-6-methylpicolinic acid, falls under the category of organic compounds. Particularly, it belongs to the class of compound known as methylpyridines. It is a pyridinecarboxylic acid with an amino group at position 4 and a methyl group at position 6. This chemical is involved in some metabolic processes. It is known to exert antibacterial and/or antifungal effects, making it potentially useful in pharmaceutical applications. The detailed properties and toxicology of this chemical is not well-known and further study is needed.

Check Digit Verification of cas no

The CAS Registry Mumber 127915-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,1 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127915-50:
(8*1)+(7*2)+(6*7)+(5*9)+(4*1)+(3*5)+(2*5)+(1*0)=138
138 % 10 = 8
So 127915-50-8 is a valid CAS Registry Number.

127915-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-6-methylnicotinic acid

1.2 Other means of identification

Product number -
Other names 4-amino-6-methylpyridine-3-carboxylic acid

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:127915-50-8 SDS

127915-50-8Relevant articles and documents

Improved Synthesis of N1-Pyridylthiamine Pyrophosphate, a Coenzymatically Active Analog of Thiamine Pyrophosphate

Neef, Holger,Golbik, Ralph,Fahlbusch, Baerbel,Schellenberger, Alfred

, p. 913 - 916 (2007/10/02)

Our previously published synthesis of the N1-pyridyl analog 1b of thiamine pyrophosphate is improved resulting in a remarkably higher yield.Key reaction of this new synthetic pathway is the oxidative degradation of 5-acetylpyridine 8 to the 5-carboxylic acid 11 via the pyridinium compound 10.Improved preparations of other intermediates are also described.The N1-pyridylthiamine pyrophosphate analog 1b has been separated and purified by ion exchange chromatography on Sephadex A-25.

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