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2051-59-4

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2051-59-4 Usage

General Description

Chlorocoumarin is a chemical compound that belongs to the coumarin family and is derived from coumarin by the addition of a chlorine atom. It is known for its wide range of biological activities, including antimicrobial, antioxidant, anti-inflammatory, and antitumor properties. Chlorocoumarin has been extensively studied for its potential therapeutic applications in the treatment of various diseases and conditions, including cancer, cardiovascular diseases, and infectious diseases. Its ability to inhibit key enzymes involved in several biological processes makes it a promising candidate for the development of new drugs and treatments. Additionally, chlorocoumarin has also shown potential as a natural food preservative and flavoring agent due to its antimicrobial and antioxidant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 2051-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2051-59:
(6*2)+(5*0)+(4*5)+(3*1)+(2*5)+(1*9)=54
54 % 10 = 4
So 2051-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H5ClO2/c10-7-2-3-8-6(5-7)1-4-9(11)12-8/h1-5H

2051-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2H-1-Benzopyran-2-one,6-chloro-

1.2 Other means of identification

Product number -
Other names 7-chloro coumarin

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:2051-59-4 SDS

2051-59-4Relevant articles and documents

Synthesis of Coumarins by Nucleophilic Denitrocyclization Reaction

Oda, Noriichi,Yoshida, Yukio,Nagai, Shin-ichi,Ueda, Taisei,Sakakibara, Jinsaku

, p. 1796 - 1802 (2007/10/02)

2-propanedioic acids(2a-c) were denitrocyclized to coumarins (3a-c) by heating in quinoline in the presence of copper powder. 2-(4-Methoxiphenyl)-3-(2-nitrophenyl)-(Z)-2-propenoic acids (6a,b,d,e) were also similarly denitrocycli

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