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

138643-95-5

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138643-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138643-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,4 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138643-95:
(8*1)+(7*3)+(6*8)+(5*6)+(4*4)+(3*3)+(2*9)+(1*5)=155
155 % 10 = 5
So 138643-95-5 is a valid CAS Registry Number.

138643-95-5SDS

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 Boc-(L)-Phe-ψ(CSNH)-(L)-Phe-OMe

1.2 Other means of identification

Product number -
Other names (S)-2-((S)-2-tert-Butoxycarbonylamino-3-phenyl-thiopropionylamino)-3-phenyl-propionic 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:138643-95-5 SDS

138643-95-5Relevant academic research and scientific papers

Endothiopeptide inhibitors of HIV-1 protease

Yao, Shao,Zutshi, Reena,Chmielewski, Jean

, p. 699 - 704 (1998)

Endothiopeptide inhibitors of HIV-1 protease were synthesized by chemical and enzymatic methods to individually replace each backbone amide bond in 1 with a thioamide-linkage. Interestingly, agent 7, which contains a thioamide-linkage between the P2

Novel approaches to optically active substituted 4,5-dihydro-1,2,4-triazin-6(1H)-ones as conformationally constrained peptidomimetics

Saniere, Laurent,Schmitt, Martine,Pellegrini, Nadia,Bourguignon, Jean-Jacques

, p. 671 - 688 (2007/10/03)

Synthesis of 4,5-dihydro-1,2,4-triazin-6-ones bearing different chiral α-amino acid residues at the C3 and N1 positions is reported. Cyclocondensation of N-thioacylphthalimides with α-amino hydrazides afforded C3 functionalised dihydrotriazinones in good

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