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L-Phenylalanine, N-[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131222-34-9

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131222-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131222-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,2 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131222-34:
(8*1)+(7*3)+(6*1)+(5*2)+(4*2)+(3*2)+(2*3)+(1*4)=69
69 % 10 = 9
So 131222-34-9 is a valid CAS Registry Number.

131222-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Nα-[N-(tert-butyloxycarbonyl)-2-aminoethyl]phenylalanine

1.2 Other means of identification

Product number -
Other names (S)-2-(2-tert-Butoxycarbonylamino-ethylamino)-3-phenyl-propionic 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:131222-34-9 SDS

131222-34-9Relevant academic research and scientific papers

Solid-phase synthesis of peptide-platinum complexes using platinum-chelating building blocks derived from amino acids

Robillard, Marc S.,Van Alphen, Sophie,Meeuwenoord, Nico J.,Jansen, Bart A. J.,Van Der Marel, Gijs A.,Van Boom, Jacques H.,Reedijk, Jan

, p. 220 - 225 (2005)

Amino acids have been employed as precursors in the synthesis of platinum-chelating solid-phase building blocks. These chelating molecules were subsequently successfully used in the solid-phase synthesis of peptide-platinum complexes. The newly introduced functionality in the chelating part, as well as the nature of the pendant peptide, was shown to have an important influence on the anticancer activity of the complexes.

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