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Alanine, 2,3-didehydro-N-[N-[(phenylmethoxy)carbonyl]-L-phenylalanyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126749-79-9

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126749-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126749-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,4 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126749-79:
(8*1)+(7*2)+(6*6)+(5*7)+(4*4)+(3*9)+(2*7)+(1*9)=159
159 % 10 = 9
So 126749-79-9 is a valid CAS Registry Number.

126749-79-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-L-Phe-ΔAla-OMe

1.2 Other means of identification

Product number -
Other names 2-((S)-2-Benzyloxycarbonylamino-3-phenyl-propionylamino)-acrylic acid methyl ester

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:126749-79-9 SDS

126749-79-9Downstream Products

126749-79-9Relevant academic research and scientific papers

An Exceptionally Mild and Efficient Route to Dehydroalanine Peptides

Ranganathan, Darshan,Shah, Kavita,Vaish, Narendra

, p. 1145 - 1147 (2007/10/02)

Δ-Ala peptides are formed in good yields on treatment of the corresponding serine precursors with oxalyl chloride and triethylamine in methylene chloride at 0 deg C.

FREE-RADICAL ADDITION TO DI- AND TRIPEPTIDES CONTAINING DEHYDROALANINE RESIDUES

Crich, David,Davies, John W.

, p. 5641 - 5654 (2007/10/02)

Radical addition, by the alkylmercury halide/sodium borohydride method, to di- and tripeptides containing a dehydroalanine residue proceeds smoothly with good chemical yield, but low diastereoselectivity, to saturated di- and tripeptides.

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