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54784-68-8

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54784-68-8 Usage

General Description

S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is a compound that plays a crucial role in various biochemical processes within the body. It is a derivative of the amino acid cysteine and contains an acetylamino group and a benzyloxy carbonyl group. S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is commonly used in the synthesis of peptides and proteins in biochemistry and pharmaceutical research. Its acetylamino group is important for modifying the structure and function of proteins, while the benzyloxy carbonyl group is often used as a protective group for thiol-containing molecules. S-[(Acetylamino)methyl]-N-[(benzyloxy)carbonyl]-L-cysteine is also utilized in the production of pharmaceutical drugs and in the study of enzyme catalysis and protein folding.

Check Digit Verification of cas no

The CAS Registry Mumber 54784-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,8 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54784-68:
(7*5)+(6*4)+(5*7)+(4*8)+(3*4)+(2*6)+(1*8)=158
158 % 10 = 8
So 54784-68-8 is a valid CAS Registry Number.

54784-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-(acetamidomethylsulfanyl)-2-(phenylmethoxycarbonylamino)propanoic acid

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:54784-68-8 SDS

54784-68-8Relevant articles and documents

A general and versatile route to "zinc finger" templates

Ranganathan, Subramania,Jayaraman, Narayanaswamy

, p. 6681 - 6682 (2007/10/02)

The basic zinc finger template is formed in a single step from PNHCys[ S- CH,2NHAc ] HisOMe and zinc chloride by a tandem complexation deprotection sequence.

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