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151255-80-0

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151255-80-0 Usage

Uses

Methyl 2,4-bis(Benzyloxy)phenylacetate is used as a reactant in the synthesis of fluorescent labeled analogs of spider toxin, NPTX-594.

Check Digit Verification of cas no

The CAS Registry Mumber 151255-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,5 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 151255-80:
(8*1)+(7*5)+(6*1)+(5*2)+(4*5)+(3*5)+(2*8)+(1*0)=110
110 % 10 = 0
So 151255-80-0 is a valid CAS Registry Number.

151255-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibenzyloxyphenylacetic acid methyl ester

1.2 Other means of identification

Product number -
Other names Methyl 2,4-Bis(benzyloxy)phenylacetate

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:151255-80-0 SDS

151255-80-0Relevant articles and documents

A MANUFACTURING PROCESS OF ISOFLAVAN OR ISOFLAVENE DERIVATIVES

-

Page/Page column 18-19, (2010/02/11)

The present invention relates to a method of synthesizing isoflavan and isoflavene derivatives of the Formula 1, which have the biological efficacy of antioxidation and protection against ultraviolet light. The method is effective and suitable for a mass production of isoflavan and isoflavene derivatives, which is a more convenient alternative preparation method compared to the isolation method by the extraction of plants, such as licorice, via troublesome preparative processes.

Synthesis and assay of hybrid analogs of argiotoxin-636 and philanthoxin-433: Glutamate receptor antagonists

Choi,Nakanishi,Usherwood

, p. 5777 - 5790 (2007/10/02)

The synthesis of the non-competitive glutamate receptor antagonist, argiotoxin-636 is described. Furthermore, synthetic routes are presented for the preparation of structural analogs including argiotoxin-philanthotoxin hybrids. Biological activities on gl

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