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136916-26-2

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136916-26-2 Usage

General Description

Boc-(S)-3-amino-2-phenylpropanoic acid is a chemical compound with the molecular formula C14H19NO4. It is a derivative of L-phenylalanine, an essential amino acid, and is commonly used in organic synthesis and peptide chemistry. The Boc group, which stands for tert-butoxycarbonyl, is often used to protect amino groups during chemical reactions. Boc-(S)-3-aMino-2-phenylpropanoic acid is largely utilized as a building block in the synthesis of various peptides and pharmaceuticals. Its ability to modify the properties of peptides makes it a valuable tool in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 136916-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,1 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136916-26:
(8*1)+(7*3)+(6*6)+(5*9)+(4*1)+(3*6)+(2*2)+(1*6)=142
142 % 10 = 2
So 136916-26-2 is a valid CAS Registry Number.

136916-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-((tert-Butoxycarbonyl)amino)-2-phenylpropanoic acid

1.2 Other means of identification

Product number -
Other names (2S)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-2-phenylpropanoic acid

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:136916-26-2 SDS

136916-26-2Downstream Products

136916-26-2Relevant articles and documents

Asymmetric synthesis of Boc-β2-homophenylglycine

Ponsinet, Rachel,Chassaing, Gerard,Lavielle, Solange

, p. 865 - 871 (1998)

Enantiomerically pure Boc-β2-homophenylglycine has been prepared in five steps starting from Oppolzer's sultam. The key step of this route is the acylation of metalated phenylacetonitrile with sultam carbonyl chloride. Subsequent reactions (reduction, N-Boc protection, oxidation of the Boc- amino alcohol) led to Boc-(S)-β2-HPhg starting from (+)-sultam.

A Heterodinuclear asymmetric catalyst for conjugate additions of α-hydroxyketones to β-substituted nitroalkenes

Trost, Barry M.,Hisaindee, Soleiman

, p. 6003 - 6005 (2007/10/03)

(Chemical Equation Presented) The bis-ProPhenol ligand was designed to facilitate formation of hetereodinuclear complexes based upon the large difference in pKa of the one phenolic OH group to the tertiary OH groups. In exploring the first exam

Palladium-catalysed asymmetric allylic substitution: Synthesis of α- and β-amino acids

Bower, Justin F.,Jumnah, Roshan,Williams, Andrew C.,Williams, Jonathan M. J.

, p. 1411 - 1420 (2007/10/03)

Methodology has been established for the formation of enantiomerically enriched α-amino acids using palladium-catalysed allylic amination. The formation of enantiomerically enriched allylamines has been achieved with high enantioselectivity. Oxidative cleavage of the allylamines provides arylglycine and glutamic acid derivatives. Additionally, enantiomerically enriched β-amino acids have been prepared in high enantiomeric excess. Palladium-catalysed asymmetric allylic substitution is used as the key synthetic transformation.

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