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Benzoic acid, 4-methoxy-2,3-dimethyl-, 2-(4-methoxy-2,3-dimethylphenyl)-2-oxoethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97900-39-5

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97900-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97900-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,0 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 97900-39:
(7*9)+(6*7)+(5*9)+(4*0)+(3*0)+(2*3)+(1*9)=165
165 % 10 = 5
So 97900-39-5 is a valid CAS Registry Number.

97900-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name O-(2,3-dimethyl-4-methoxybenzoyl)-ω-hydroxy-2,3-dimethyl-4-methoxyacetophenone

1.2 Other means of identification

Product number -
Other names -

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:97900-39-5 SDS

97900-39-5Relevant academic research and scientific papers

PHENYLETHANOLAMINE DERIVATIVES, III. SYNTHESIS OF 1-(HYDROXY- AND METHOXYPHENYL)-2-AMINOETHANOL DERIVATIVES

Hajoos, Andor

, p. 63 - 70 (2007/10/02)

New 1-(methoxyphenyl)- and 1-(hydroxyphenyl)-2-aminoethanol derivatives have been prepared for the purpose of biological testing.The compounds were obtained via aminolysis of the corresponding phenacyl halides and subsequent reduction of the resulting phenacylamines with sodium tetrahydridoborate.In the aminolysis of phenacyl halides O-benzoyl-ω-hydroxyaminoacetophenones and 1,2-dibenzoylethanes were formed as by-products.In some cases the 4-methoxy-ω-aminoacetophenones were hydrolyzed by aqueous hydrogen bromide into the corresponding glycine and phenol.

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