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137828-53-6

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137828-53-6 Usage

General Description

BOC-PHE-(R)-VAL-OH is a chemical compound consisting of protected amino acids. The BOC group serves as a protective moiety for the amino group of phenylalanine and valine, while the (R) configuration indicates the stereochemistry of the valine residue. BOC-PHE-(R)-VAL-OH is commonly used in peptide synthesis and solid-phase peptide synthesis, where the BOC group can be selectively removed to expose the free amino group for further reactions. It is also involved in the production of pharmaceuticals and medicinal chemistry research. Overall, BOC-PHE-(R)-VAL-OH is a crucial building block in the creation of peptide and protein structures for various applications in the field of chemistry and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 137828-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,8,2 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137828-53:
(8*1)+(7*3)+(6*7)+(5*8)+(4*2)+(3*8)+(2*5)+(1*3)=156
156 % 10 = 6
So 137828-53-6 is a valid CAS Registry Number.

137828-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-PHE-(R)-VAL-OH

1.2 Other means of identification

Product number -
Other names -

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:137828-53-6 SDS

137828-53-6Downstream Products

137828-53-6Relevant articles and documents

Conformational analysis of a cyclic RGD peptide containing a Ψ[CH2-NH] bond: A positional shift in backbone structure caused by a single dipeptide mimetic

Geyer, Armin,Müller, Gerhard,Kessler, Horst

, p. 7735 - 7743 (2007/10/02)

The pseudopentapeptide cyclo(-Arg1-Gly2-Asp3-D-Phe4Ψ[CH2-NH]Val5-) (1) was synthesized by a combination of solution and solid-phase methods. The reduced peptide bond was incorporated as a dipeptide bu

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