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3-Chloro-L-tyrosine, a chlorinated derivative of the amino acid L-tyrosine, is a chemical compound characterized by the presence of a chlorine atom attached to the carbon atom in the para position of the phenol ring. It plays a significant role in organic synthesis and holds potential in the development of pharmaceutical compounds.

70680-93-2

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70680-93-2 Usage

Uses

Used in Organic Synthesis:
3-Chloro-L-tyrosine is used as a building block for the creation of new pharmaceutical compounds and other chemical reactions, contributing to the advancement of medicinal chemistry.
Used in Pharmaceutical Industry:
3-Chloro-L-tyrosine is used as a precursor for the synthesis of specific drugs, highlighting its importance in the development of novel therapeutic agents.
Used in Anti-Cancer Research:
3-Chloro-L-tyrosine is studied for its potential therapeutic applications, particularly in the development of new anti-cancer agents, showcasing its promise in cancer treatment and research.

Check Digit Verification of cas no

The CAS Registry Mumber 70680-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,8 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70680-93:
(7*7)+(6*0)+(5*6)+(4*8)+(3*0)+(2*9)+(1*3)=132
132 % 10 = 2
So 70680-93-2 is a valid CAS Registry Number.

70680-93-2SDS

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-chloro-4-hydroxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 3-Chlorotyrosine

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:70680-93-2 SDS

70680-93-2Downstream Products

70680-93-2Relevant academic research and scientific papers

Vinylation of Unprotected Phenols Using a Biocatalytic System

Busto, Eduardo,Simon, Robert C.,Kroutil, Wolfgang

, p. 10899 - 10902 (2015)

Readily available substituted phenols were coupled with pyruvate in buffer solution under atmospheric conditions to afford the corresponding para-vinylphenol derivatives while releasing only one molecule of CO2 and water as the by-products. This transformation was achieved by designing a biocatalytic system that combines three biocatalytic steps, namely the C-C coupling of phenol and pyruvate in the presence of ammonia, which leads to the corresponding tyrosine derivative, followed by deamination and decarboxylation. The biocatalytic transformation proceeded with high regioselectivity and afforded exclusively the desired para products. This method thus represents an environmentally friendly approach for the direct vinylation of readily available 2-, 3-, or 2,3-disubstituted phenols on preparative scale (0.5 mmol) that provides vinylphenols in high yields (65-83%).

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