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142955-51-9

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142955-51-9 Usage

General Description

BOC-PHE-N-CARBOXYANHYDRIDE, also known as Boc-phenylalanine N-carboxyanhydride, is a chemical compound used in peptide synthesis. It is a derivative of the amino acid phenylalanine and is commonly used as a coupling reagent to form peptide bonds during the solid-phase synthesis of peptides. BOC-PHE-N-CARBOXYANHYDRIDE acts as a protecting group for the side chain of phenylalanine, allowing for selective deprotection and coupling reactions. It is a valuable tool in the production of peptides for use in pharmaceuticals, biotechnology, and research.

Check Digit Verification of cas no

The CAS Registry Mumber 142955-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 142955-51:
(8*1)+(7*4)+(6*2)+(5*9)+(4*5)+(3*5)+(2*5)+(1*1)=139
139 % 10 = 9
So 142955-51-9 is a valid CAS Registry Number.

142955-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-PHE-N-CARBOXYANHYDRIDE

1.2 Other means of identification

Product number -
Other names Boc-Phe-NCA

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:142955-51-9 SDS

142955-51-9Relevant articles and documents

Asymmetric synthesis of α-amino acids via cinchona alkaloid-catalyzed kinetic resolution of urethane-protected α-amino acid N-carboxyanhydrides

Hang,Tian,Tang,Deng

, p. 12696 - 12697 (2007/10/03)

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N-Alkoxycarbonyl Amino Acid N-Carboxyanhydrides and N,N-Dialkoxycarbonyl Amino Acid Fluorides from N,N-Diprotected Amino Acids

Savrda, J.,Wakselman, M.

, p. 812 - 813 (2007/10/02)

Activation of N,N-bis-Boc or N-Boc N-Z amino acids with SOCl2-DMF leads to N-protected N-carboxy amino acid anhydrides, whereas treatment with cyanuric fluoride at low temperature gives mainly N,N-bis-protected amino acid fluorides, which are efficient ac

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