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139393-81-0

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139393-81-0 Usage

General Description

2(1H)-Pyridinone, 5-ethyl-6-methyl-3-nitro- is a chemical compound with the molecular formula C9H10N2O3. It is a derivative of pyridinone and is characterized by the presence of a nitro group, an ethyl group, and a methyl group on the pyridinone ring. 2(1H)-Pyridinone, 5-ethyl-6-methyl-3-nitro- is commonly used in the pharmaceutical industry as a building block for the synthesis of various organic compounds. It exhibits pharmacological properties and can potentially be used in the development of new drugs. Additionally, the presence of the nitro group makes this compound useful in the synthesis of other valuable chemical intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 139393-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,9 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 139393-81:
(8*1)+(7*3)+(6*9)+(5*3)+(4*9)+(3*3)+(2*8)+(1*1)=160
160 % 10 = 0
So 139393-81-0 is a valid CAS Registry Number.

139393-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethyl-6-methyl-3-nitro-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 3-nitro-5-ethyl-6-methylpyridin-2(1H)-one

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:139393-81-0 SDS

139393-81-0Relevant articles and documents

Novel ring transformation of nitropyrimidinone; synthetic equivalent of α-nitroformylacetic acid

Nishiwaki, Nagatoshi,Wang, Hui-Ping,Matsuo, Kengo,Tohda, Yasuo,Ariga, Masahiro

, p. 2261 - 2262 (1997)

3-Methyl-5-nitropyrimidin-4(3H)-one reacts with ketones in the presence of ammonium salts to afford disubstituted pyrimidines and disubstituted 3-nitro-2-pyridones in a novel ring transformation reaction; nitropyrimidinone behaves as an activated diformylamine in the former case, and as a synthetic equivalent of α-nitroformylacetic acid in the latter case.

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