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57096-11-4

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57096-11-4 Usage

Description

Boc-N'-(2-chloro-Cbz)-D-lysine, also known as Boc-D-Lys(2-Cl-Z)-OH, is an amino acid derivative characterized by its white powder form. It is a modified version of the naturally occurring amino acid, D-lysine, with the addition of a 2-chlorobenzyloxycarbonyl (Cbz) group and a tert-butyloxycarbonyl (Boc) group. These modifications enhance its reactivity and stability in various chemical and biological processes.

Uses

Used in Chemical Synthesis:
Boc-N'-(2-chloro-Cbz)-D-lysine is used as a building block in chemical synthesis for the creation of complex organic molecules. Its unique structure allows for specific reactions and modifications, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Peptide Chemistry:
In peptide chemistry, Boc-N'-(2-chloro-Cbz)-D-lysine is utilized as a protected amino acid for the synthesis of peptides and proteins. The protective groups (Boc and Cbz) prevent unwanted side reactions during the peptide assembly process, ensuring the correct formation of peptide bonds and the desired final product. This application is particularly relevant in the development of therapeutic peptides, diagnostic agents, and research tools.
Used in Pharmaceutical Industry:
Boc-N'-(2-chloro-Cbz)-D-lysine is used as an intermediate in the pharmaceutical industry for the development of new drugs. Its unique chemical properties enable the creation of novel drug candidates with potential applications in various therapeutic areas, such as oncology, cardiovascular diseases, and neurological disorders.
Used in Research and Development:
In the field of research and development, Boc-N'-(2-chloro-Cbz)-D-lysine serves as a valuable tool for studying the structure and function of proteins and peptides. Its use in the synthesis of modified peptides allows researchers to investigate the effects of specific amino acid modifications on protein function, stability, and interactions with other biomolecules.

Check Digit Verification of cas no

The CAS Registry Mumber 57096-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,9 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57096-11:
(7*5)+(6*7)+(5*0)+(4*9)+(3*6)+(2*1)+(1*1)=134
134 % 10 = 4
So 57096-11-4 is a valid CAS Registry Number.

57096-11-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H63069)  Nalpha-Boc-Nepsilon-(2-chlorobenzyloxycarbonyl)-D-lysine, 98%   

  • 57096-11-4

  • 1g

  • 324.0CNY

  • Detail
  • Alfa Aesar

  • (H63069)  Nalpha-Boc-Nepsilon-(2-chlorobenzyloxycarbonyl)-D-lysine, 98%   

  • 57096-11-4

  • 5g

  • 1294.0CNY

  • Detail
  • Aldrich

  • (15084)  Boc-D-Lys(2-Cl-Z)-OH  ≥98.0% (TLC)

  • 57096-11-4

  • 15084-5G-F

  • 1,813.50CNY

  • Detail

57096-11-4SDS

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-N-(2-Chloro-Cbz)-D-Lysine

1.2 Other means of identification

Product number -
Other names (2R)-6-[(2-chlorophenyl)methoxycarbonylamino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic 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:57096-11-4 SDS

57096-11-4Upstream product

57096-11-4Relevant articles and documents

Fatty acid analogs and prodrugs

-

, (2008/06/13)

Novel derivatives of fatty acid analogs that have from one to three heteroatoms in the fatty acid moiety which can be oxygen, sulfur or nitrogen, are disclosed in which the carboxy-terminus has been modified to form various amides, esters, ketones, alcohols, alcohol esters and nitrites thereof. These compounds are useful as substrates for N-myristoyltransferase (NMT) and/or its acyl coenzyme, and as anti-viral and anti-fungal agents or pro-drugs of such agents. Illustrative of the disclosed compounds are fatty acid amino acid analogs of the structure STR1 in which x is the ethyl or t-butyl ester of an amino acid such as Gly, L-Ala, L-Ile, L-Phe, L-Trp, L-Thr or an amide such as NHCH2 C6 H5 or NH(CH2)2 C6 H5.

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