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CHLOROAC-ASP-OH is a chemical compound derived from aspartic acid, featuring a chloroacetyl group. It is known for its ability to selectively react with amino groups on peptides and proteins, making it a valuable tool for the modification and functionalization of biomolecules. Its selective targeting capability and potential to disrupt protein-protein interactions have also positioned it as a candidate for drug development and cancer treatment.
Used in Pharmaceutical Industry:
CHLOROAC-ASP-OH is used as a coupling reagent in peptide synthesis for the formation of peptide bonds. Its selective reactivity with amino groups facilitates the creation of specific peptide sequences, which is crucial for the development of new drugs and therapeutic agents.
Used in Biomedical Research:
CHLOROAC-ASP-OH is used as a research tool for the modification and functionalization of biomolecules. Its ability to selectively target specific amino acid residues aids in the study of protein interactions and the development of targeted therapies.
Used in Drug Development:
CHLOROAC-ASP-OH is used as a potential therapeutic agent in the field of drug development. Its capacity to selectively target and disrupt protein-protein interactions makes it a promising candidate for the creation of new treatments, particularly in the area of cancer therapy.

67036-33-3

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67036-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67036-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,3 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67036-33:
(7*6)+(6*7)+(5*0)+(4*3)+(3*6)+(2*3)+(1*3)=123
123 % 10 = 3
So 67036-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8ClNO5/c7-2-4(9)8-3(6(12)13)1-5(10)11/h3H,1-2H2,(H,8,9)(H,10,11)(H,12,13)

67036-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name CHLOROAC-ASP-OH

1.2 Other means of identification

Product number -
Other names N-Chloracetyl-asparaginsaeure

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:67036-33-3 SDS

67036-33-3Relevant academic research and scientific papers

Process for preparing diketopiperazine derivatives

-

, (2008/06/13)

A diketopiperazine derivative is prepared by reacting chloroacetylaspartic acid with ammonia water, diesterifying the resulting glycyl-aspartic acid with an alkanol, and then cyclizing the diester in neutral or weakly basic water or in an alkanol-water solvent mixture.

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