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Benzoic acid, 2-hydroxy-4-(phenylmethoxy)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97476-06-7

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97476-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97476-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,7 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97476-06:
(7*9)+(6*7)+(5*4)+(4*7)+(3*6)+(2*0)+(1*6)=177
177 % 10 = 7
So 97476-06-7 is a valid CAS Registry Number.

97476-06-7SDS

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 benzyl 2-hydroxy-4-phenylmethoxybenzoate

1.2 Other means of identification

Product number -
Other names Benzyl 4-benzyloxy-2-hydroxybenzoate

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:97476-06-7 SDS

97476-06-7Relevant academic research and scientific papers

Anacardic acid derived salicylates are inhibitors or activators of lipoxygenases

Wisastra, Rosalina,Ghizzoni, Massimo,Boltjes, Andre,Haisma, Hidde J.,Dekker, Frank J.

supporting information; experimental part, p. 5027 - 5032 (2012/09/22)

Lipoxygenases catalyze the oxidation of unsaturated fatty acids, such as linoleic acid, which play a crucial role in inflammatory responses. Selective inhibitors may provide a new therapeutic approach for inflammatory diseases. In this study, we describe

Highly efficient and chemoselective cleavage of prenyl ethers using ZrCl4/NaBH4

Suresh Babu,China Raju,Srinivas,Madhusudana Rao

, p. 2525 - 2528 (2007/10/03)

An efficient and chemoselective deprotection of prenyl ethers of phenols and alcohols with ZrCl4/NaBH4 in DCM was achieved in high yields. The selectivity of prenyl ether deprotection is well demonstrated by carrying out the reaction

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