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Glycine, N-[N-[N-[N-[(1,1-dimethylethoxy)carbonyl]-L-2-phenylglycyl]-L-phenylalan yl]-L-phenylalanyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139151-81-8

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139151-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139151-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,5 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 139151-81:
(8*1)+(7*3)+(6*9)+(5*1)+(4*5)+(3*1)+(2*8)+(1*1)=128
128 % 10 = 8
So 139151-81-8 is a valid CAS Registry Number.

139151-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Phg-Phe-Phe-Gly-OH

1.2 Other means of identification

Product number -
Other names {(S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-2-phenyl-acetylamino)-3-phenyl-propionylamino]-3-phenyl-propionylamino}-acetic 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:139151-81-8 SDS

139151-81-8Downstream Products

139151-81-8Relevant academic research and scientific papers

SYNTHESIS OF A NUMBER OF COMBINED ANALOGUES OF SUBSTANCE P AND LITORIN

Galyuk, E. N.,Egorova, S. V.,Gurina, E. B.,Golubovich, V. P.,Akhrem, A. A.

, p. 94 - 98 (2007/10/02)

With the aim of obtaining new biologically active compounds, we have synthesized nine combined peptides (I)-(IX) consisting of combinations of the C-terminal tripeptide litorin and the hydrophobic central fragments of substance P, and also modified analogues of them.The synthesis of these compounds was achieved by the methods of classical peptide chemistry with the condensation of their N-terminal moieties with the C-terminal tripeptide H-His-Phe-Met-NH2.

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