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127915-47-3

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127915-47-3 Usage

General Description

Ethanone, 1-(4-amino-6-methyl-3-pyridinyl)- is a chemical compound with the molecular formula C8H10N2O. Also known as 4-Amino-6-methyl-3-pyridinyl methyl ketone, it is a pyridinyl compound with a ketone functional group. This chemical is commonly used in the synthesis of pharmaceuticals and agricultural chemicals. It is also used as an intermediate in the production of various organic compounds. 4-Amino-6-methyl-3-pyridinyl methyl ketone is a versatile building block in organic chemistry and is important in the production of drugs and other biologically active molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 127915-47-3 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, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127915-47:
(8*1)+(7*2)+(6*7)+(5*9)+(4*1)+(3*5)+(2*4)+(1*7)=143
143 % 10 = 3
So 127915-47-3 is a valid CAS Registry Number.

127915-47-3SDS

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 1-(4-amino-6-methylpyridin-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 5-Acetyl-4-amino-2-methylpyridin

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:127915-47-3 SDS

127915-47-3Relevant 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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