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2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI) is a chemical compound with the molecular formula C9H5ClN2O2S. It is a derivative of benzothiazolecarboxylic acid with a chlorine substituent at the sixth position. 2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI) is known for its potential biological activities and therapeutic effects, making it a valuable compound in drug discovery and development. The chloro substituent can alter the physicochemical properties and biological activities of the parent compound, leading to enhanced or novel pharmacological effects.

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  • 3622-03-5 Structure
  • Basic information

    1. Product Name: 2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI)
    2. Synonyms: 2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI);6-Chlorobenzo[d]thiazole-2-carboxylic acid;6-chloro-1,3-benzothiazole-2-carboxylic acid
    3. CAS NO:3622-03-5
    4. Molecular Formula: C8H4ClNO2S
    5. Molecular Weight: 213.644
    6. EINECS: N/A
    7. Product Categories: BENZOTHIAZOLE
    8. Mol File: 3622-03-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 411.675°C at 760 mmHg
    3. Flash Point: 202.774°C
    4. Appearance: /
    5. Density: 1.634g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.734
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI)(3622-03-5)
    12. EPA Substance Registry System: 2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI)(3622-03-5)
  • 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: 3622-03-5(Hazardous Substances Data)

3622-03-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI) is used as a building block for the synthesis of various drugs and pharmaceuticals. Its potential biological activities and therapeutic effects make it an important compound in drug discovery and development.
Used in Drug Discovery and Development:
2-Benzothiazolecarboxylicacid,6-chloro-(6CI,7CI,8CI) is used as a valuable compound in drug discovery and development due to its potential biological activities and therapeutic effects. The chloro substituent can enhance or provide novel pharmacological effects, making it a promising candidate for the development of new drugs and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 3622-03-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,2 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3622-03:
(6*3)+(5*6)+(4*2)+(3*2)+(2*0)+(1*3)=65
65 % 10 = 5
So 3622-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H4ClNO2S/c9-4-1-2-5-6(3-4)13-7(10-5)8(11)12/h1-3H,(H,11,12)

3622-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chlorobenzo[d]thiazole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-Chloro-1,3-benzothiazole-2-carboxylic acid

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:3622-03-5 SDS

3622-03-5Downstream Products

3622-03-5Relevant articles and documents

Direct C-H carboxylation with carbon dioxide using 1,2,3-triazol-5-ylidene copper(I) complexes

Inomata, Hiroshi,Ogata, Kenichi,Fukuzawa, Shin-Ichi,Hou, Zhaomin

supporting information; experimental part, p. 3986 - 3989 (2012/09/10)

1,2,3-Triazol-5-ylidene copper(I) complexes (tzNHC-Cu) efficiently catalyzed the direct C-H carboxylation of benzoxazole and benzothiazole derivatives with CO2 to give the corresponding esters in excellent yields after treatment with alkyl iodi

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