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2-Butenoic acid, 3-(2-naphthalenyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51212-51-2

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51212-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51212-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,1 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51212-51:
(7*5)+(6*1)+(5*2)+(4*1)+(3*2)+(2*5)+(1*1)=72
72 % 10 = 2
So 51212-51-2 is a valid CAS Registry Number.

51212-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-naphthalen-2-ylbut-2-enoate

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:51212-51-2 SDS

51212-51-2Relevant academic research and scientific papers

Inhibition of telomerase by BIBR 1532 and related analogues

Barma,Elayadi, Anissa,Falck,Corey, David R.

, p. 1333 - 1336 (2007/10/03)

BIBR 1532 has been reported to be a potent, small molecule inhibitor of human telomerase, suggesting it as a lead for the development of anti-telomerase therapy. We confirm the ability of BIBR 1532 to inhibit telomerase and report the discovery of an equa

A phosphane-free catalyst system for the heck arylation of disubstituted alkenes: Application to the synthesis of trisubstituted olefins

Guertler, Christoph,Buchwald, Stephen L.

, p. 3107 - 3112 (2007/10/03)

A new general procedure for the Heck arylation of disubstituted olefins is described. This procedure allows, in many instances, the stereoselective synthesis of trisubstituted olefins. Trisubstituted olefins are easily accessible under mild reaction condi

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