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90873-00-0

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90873-00-0 Usage

General Description

N-(5-ethyl-2-Methylpyridin-4-yl)acetamide is a chemical compound with the molecular formula C11H15N3O. It is a derivative of pyridine and is commonly used in pharmaceutical research and drug development. N-(5-ethyl-2-Methylpyridin-4-yl)acetaMide has been studied for its potential role in treating various medical conditions such as neurodegenerative diseases, cancer, and inflammation. It is also used as a building block in organic synthesis to create other pharmaceutical compounds. N-(5-ethyl-2-Methylpyridin-4-yl)acetamide is known for its ability to modulate biological processes and has shown promise in preclinical studies for potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 90873-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90873-00:
(7*9)+(6*0)+(5*8)+(4*7)+(3*3)+(2*0)+(1*0)=140
140 % 10 = 0
So 90873-00-0 is a valid CAS Registry Number.

90873-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-ethyl-2-methylpyridin-4-yl)acetamide

1.2 Other means of identification

Product number -
Other names 4-Acetamino-2-methyl-5-ethyl-pyridin

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:90873-00-0 SDS

90873-00-0Relevant 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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