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Chlorocoumarin, a member of the coumarin family, is a chemical compound derived from coumarin with the addition of a chlorine atom. It exhibits a broad spectrum of biological activities, such as antimicrobial, antioxidant, anti-inflammatory, and antitumor properties. Its potential therapeutic applications span across the treatment of various diseases and conditions, including cancer, cardiovascular diseases, and infectious diseases. Chlorocoumarin's capacity to inhibit key enzymes in several biological processes positions it as a promising candidate for the development of new drugs and treatments. Furthermore, it has demonstrated potential as a natural food preservative and flavoring agent due to its antimicrobial and antioxidant properties.

2051-59-4

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2051-59-4 Usage

Uses

Used in Pharmaceutical Industry:
Chlorocoumarin is used as a therapeutic agent for the treatment of various diseases and conditions, such as cancer, cardiovascular diseases, and infectious diseases, due to its antimicrobial, antioxidant, anti-inflammatory, and antitumor properties.
Used in Food Industry:
Chlorocoumarin is used as a natural food preservative and flavoring agent, leveraging its antimicrobial and antioxidant properties to enhance food safety and quality.
Used in Drug Development:
Chlorocoumarin is utilized in the development of new drugs and treatments, capitalizing on its ability to inhibit key enzymes involved in several biological processes.

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 academic research and scientific papers

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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