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82278-95-3

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82278-95-3 Usage

General Description

Boc-L-3-Bromophenylalanine is a chemical compound that consists of a protection group (Boc) attached to the amino acid L-3-Bromophenylalanine. L-3-Bromophenylalanine is a derivative of the amino acid phenylalanine, in which the hydrogen atom at the alpha carbon is substituted by a bromine atom. Boc-L-3-Bromophenylalanine is commonly used in peptide synthesis and as a building block for the preparation of peptide-based drugs and pharmaceuticals. The Boc protection group helps to prevent unwanted side reactions during the synthesis of peptides, making Boc-L-3-Bromophenylalanine a useful tool in the field of chemical biology and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 82278-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,7 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82278-95:
(7*8)+(6*2)+(5*2)+(4*7)+(3*8)+(2*9)+(1*5)=153
153 % 10 = 3
So 82278-95-3 is a valid CAS Registry Number.

82278-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-L-3-Bromophenylalanine

1.2 Other means of identification

Product number -
Other names 3-(3-bromophenyl)pro-2-yn-1-ol

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:82278-95-3 SDS

82278-95-3Relevant articles and documents

Hydroxyethylene sulfones as a new scaffold to address aspartic proteases: Design, synthesis, and structural characterization

Specker, Edgar,B?ttcher, Jark,Heine, Andreas,Sotriffer, Christoph A.,Lilie, Hauke,Schoop, Andreas,Müller, Gerhard,Griebenow, Nils,Klebe, Gerhard

, p. 6607 - 6619 (2007/10/03)

Hydroxyethylene sulfones were developed as novel scaffolds against aspartyl proteases. A diastereoselective synthesis has been established to introduce the required side chain decoration with desired stereochemistry. Depending on the substitution of the h

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