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1131-20-0

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1131-20-0 Usage

General Description

3-Ethyl-6-methyl-4-nitro-6H-pyridine 1-oxide is a chemical compound with the molecular formula C8H10N2O3. It is a nitroso compound, and its structure contains a six-membered pyridine ring with an ethyl group at the 3-position, a methyl group at the 6-position, and a nitroso group at the 4-position. 3-ethyl-6-methyl-4-nitro-6H-pyridine 1-oxide is widely used in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. It is also known for its ability to act as a radical scavenger and an antioxidant, making it useful in the formulation of cosmetics and other personal care products. Additionally, its structural and electronic properties make it a valuable tool for the investigation of chemical reactions and mechanisms in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1131-20-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1131-20:
(6*1)+(5*1)+(4*3)+(3*1)+(2*2)+(1*0)=30
30 % 10 = 0
So 1131-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N2O3/c1-3-7-5-9(11)6(2)4-8(7)10(12)13/h4-6H,3H2,1-2H3/q+1

1131-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethyl-2-methyl-4-nitro-1-oxidopyridin-1-ium

1.2 Other means of identification

Product number -
Other names 2-Methyl-5-ethyl-4-nitropyridin-N-oxid

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 -
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More Details:1131-20-0 SDS

1131-20-0Relevant 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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