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3,6-DIMETHYLPYRAZINE-2,5-DIOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89532-72-9

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89532-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89532-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89532-72:
(7*8)+(6*9)+(5*5)+(4*3)+(3*2)+(2*7)+(1*2)=169
169 % 10 = 9
So 89532-72-9 is a valid CAS Registry Number.

89532-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-3,6-dimethyl-1H-pyrazin-2-one

1.2 Other means of identification

Product number -
Other names 3,6-Dihydroxy-2,5-dimethyl-pyrazin

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:89532-72-9 SDS

89532-72-9Downstream Products

89532-72-9Relevant academic research and scientific papers

Studies on Pyrazines. 15. A Convenient Synthesis of 2,5-Dihydroxypyrazines

Sato, Nobuhiro,Kato, Yukihiro

, p. 1677 - 1680 (2007/10/02)

The reaction of 2,5-dimethoxypyrazines with iodotrimethylsilane followed by hydrolysis was investigated to prepare the title compounds.

Studies on Pyrazines. 14. The Syntheses of 2,5-Dihydroxypyrazines and Their Derivatives

Adachi, Jiro,Sato, Nobuhiro

, p. 871 - 875 (2007/10/02)

Reaction of phenylglycinamide (1c) with ethyl benzoylformate (2c) in the presence of refluxing ethanolic sodium ethoxide gave 2,5-dihydroxy-3,6-diphenylpyrazine (3i) in 19percent yield.This synthetic method, howewer, was limited to the preparation of 3i.On the other hand, α-aminoamides 1 condensed with α-ketoesters 2 to give the intermediates 5, which were also prepared by condensation of 1 with α-ketalesters 6, followed by hydrolysis of the ketal moeity.Cyclization of 5 with refluxing methanolic sodium methoxide gave only disubstituted 2,5-dihydroxypyrazines 3.Acetylation of 5 with refluxing acetic anhydride/acetic acid led to direct formation of 2,5-diacetoxypyrazines 9.Similarly, compounds 5 could be converted into 2,5-dichloropyrazines 4.

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