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2-Chloro-L-phenylalanine is an amino acid derivative characterized by the presence of a chlorine atom at the 2-position on the phenylalanine molecule. It is recognized for its role in the synthesis of pharmaceuticals and agrochemicals, and as a potential building block for the modification of proteins and peptides. 2-CHLORO-L-PHENYLALANINE has demonstrated significant biological activity, particularly as a protein inhibitor, which has made it a subject of interest in medical research focused on cancer and enzyme inhibition. Furthermore, 2-Chloro-L-phenylalanine is utilized in the investigation of the structure-function relationships of enzymes and protein-protein interactions, although its potential hazardous properties necessitate careful handling.

185030-83-5

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185030-83-5 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Chloro-L-phenylalanine is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Production:
This amino acid derivative is also utilized in the production of agrochemicals, where it may enhance the effectiveness of certain agricultural products.
Used in Cancer Research:
In the field of medical research, 2-Chloro-L-phenylalanine is employed as a protein inhibitor, which has shown promise in studies related to cancer treatment, potentially leading to the development of novel cancer therapies.
Used in Enzyme Inhibition Studies:
2-CHLORO-L-PHENYLALANINE is used as a tool in enzyme inhibition studies, helping researchers understand the mechanisms by which certain enzymes are regulated and how they can be targeted for therapeutic purposes.
Used in Protein and Peptide Modification:
2-Chloro-L-phenylalanine serves as a building block for the modification of proteins and peptides, allowing for the exploration of new protein functions and applications in biotechnology.
Used in Enzyme and Protein Interaction Research:
2-CHLORO-L-PHENYLALANINE is utilized in the study of enzyme and protein interactions, providing insights into the structural and functional aspects of these biological processes, which is crucial for advancing our understanding of various diseases and their treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 185030-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,0,3 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 185030-83:
(8*1)+(7*8)+(6*5)+(5*0)+(4*3)+(3*0)+(2*8)+(1*3)=125
125 % 10 = 5
So 185030-83-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H10ClNO2.ClH/c10-7-4-2-1-3-6(7)5-8(11)9(12)13;/h1-4,8H,5,11H2,(H,12,13);1H/t8-;/m0./s1

185030-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-(2-chlorophenyl)propanoic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names I01-9234

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:185030-83-5 SDS

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