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92714-95-9

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92714-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92714-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,1 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92714-95:
(7*9)+(6*2)+(5*7)+(4*1)+(3*4)+(2*9)+(1*5)=149
149 % 10 = 9
So 92714-95-9 is a valid CAS Registry Number.

92714-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(2-hydroxy-4-methoxyphenyl)-3-oxo-2-phenylpropyl] acetate

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:92714-95-9 SDS

92714-95-9Downstream Products

92714-95-9Relevant articles and documents

Enzyme-catalyzed chemoselective transesterification reactions on hydroxymethylated phenolic compounds

Parmar, Virinder S.,Prasad, Ashok K.,Pati, Hari N.,Kumar, Rajesh,Azim, Abul,Roy, Sucharita,Errington, William

, p. 119 - 134 (2007/10/03)

The chemoselective capabilities of porcine pancreatic lipase (PPL) in tetrahydrofuran and Candida rugosa lipase (CRL) in diisopropyl ether have been investigated for selective acetylation and deacetylation of hydroxymethylated phenols and hydroxyaryl alky

A New Synthesis of Isoflavanones

Jain, A. C.,Sharma, Anita

, p. 451 - 452 (2007/10/02)

7-Methoxy-(3a)- and 5,7-dimethoxy-(3b)-isoflavanones have been synthesised in good yields by reacting corresponding o-hydroxydesoxybenzoins (1) with ethoxymethyl chloride in the presence of boiling acetone and dry potassium carbonate, followed by refluxing with ethanolic 4 percent aq. sodium carbonate.The products of the first step have been isolated as α-hydroxymethyldesoxybenzoins (2) and explanation of their formation is provided.

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