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103620-90-2

6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103620-90-2 Structure

  • Basic information

    1. Product Name: 6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one
    2. Synonyms: 6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one
    3. CAS NO:103620-90-2
    4. Molecular Formula: C9H5 Cl O4
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103620-90-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 335.8°Cat760mmHg
    3. Flash Point: 156.9°C
    4. Appearance: /
    5. Density: 1.786g/cm3
    6. Vapor Pressure: 4.6E-05mmHg at 25°C
    7. Refractive Index: 1.736
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one(103620-90-2)
    12. EPA Substance Registry System: 6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one(103620-90-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 103620-90-2(Hazardous Substances Data)

103620-90-2 Usage

General Description

6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one, also known as Cloricromene, is a chemical compound with the molecular formula C9H5ClO4. It is a synthetic derivative of coumarin and belongs to the class of benzopyran-2-one compounds. Cloricromene is known for its antioxidant and anti-inflammatory properties, making it a potential candidate for the treatment of cardiovascular diseases and other inflammatory conditions. It is also being studied for its potential use in the prevention and treatment of thrombotic disorders. Additionally, Cloricromene has been found to have protective effects on the liver and has shown potential as an antidiabetic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 103620-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,2 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103620-90:
(8*1)+(7*0)+(6*3)+(5*6)+(4*2)+(3*0)+(2*9)+(1*0)=82
82 % 10 = 2
So 103620-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H5ClO4/c10-4-1-2-6-5(3-4)7(11)8(12)9(13)14-6/h1-3,12-13H

103620-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-3,4-dihydroxychromen-2-one

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran-2-one,6-chloro-3,4-dihydroxy

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:103620-90-2 SDS

103620-90-2Downstream Products

103620-90-2Relevant articles and documents

Aci-reductone compounds belonging to the 6,7-disubstituted-3,4-dihydro benzopyan-2H-one class having antiaggregatory properties

-

, (2008/06/13)

The present invention relates to novel benzopyranone aci-reductone compounds of the formula I wherein X and Y are selected from the group comprising H (except that X and Y are not both H, unless otherwise indicated) Cl or other halogen, OH, a straight or

Synthetic aci-Reductones: 3,4-Dihydroxy-2H-1-benzopyran-2-ones and Their cis- and trans-4a,5,6,7,8,8a-Hexahydro Diastereomers. Antiaggregatory, Antilipidemic, and Redox Properties Compared to Those of the 4-Substituted 2-Hydroxytetronic Acids

Witiak, Donald T.,Kim, Sung K.,Tehim, Ashok K.,Sternitzke, Kent D.,McCreery, Richard L.,et al.

, p. 1437 - 1445 (2007/10/02)

Synthetic procedures for the elaboration of aci-reductones belonging to the 6- or 7-mono- or bis-substituted-3,4-dihydroxy-2H-1-benzopyran-2-ones (6 - 10) and their cis- and trans-4a,5,6,7,8,8a-hexahydro diastereomers (11, 12) are described.Hexahydrobenzo

Comparative Antiaggregatory Activity in Human Platelets of a Benzopyranone aci-Reductone, Clofibric Acid, and a 2,3-Dihydrobenzofuran Analogue

Witiak, Donald T.,Kim, Sung K.,Romstedt, Karl,Newman, Howard A. I.,Feller, Dennis R.

, p. 2170 - 2174 (2007/10/02)

A synthetic method for the preparation of aci-reductone 6-chloro-3,4-dihydroxy-2H-1-benzopyran-2-one (3) from 5-chlorosalicylate is presented.In human platelets, the benzopyranone derivative 3, clofibric acid (1), and the 2,3-dihydrobenzofuran analogue 4

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