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Tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate is a white solid chemical compound belonging to the class of organic compounds known as isothiazoles. It has the molecular formula C14H14BrNO2S and a molecular weight of 330.23 g/mol. tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate is commonly used in medicinal chemistry and drug development as a potential building block for the synthesis of bioactive molecules. Its isothiazole ring system is known for its bioactivity, and the presence of a tert-butyl group provides steric hindrance, which can enhance its biological activity and selectivity.

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  • 932702-07-3 Structure
  • Basic information

    1. Product Name: tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate
    2. Synonyms: tert-butyl 6-bromobenzo[d]isothiazole-3-carboxylate;6-Bromo-1,2-benzisothiazole-3-carboxylic acid 1,1-dimethylethyl ester
    3. CAS NO:932702-07-3
    4. Molecular Formula: C12H12BrNO2S
    5. Molecular Weight: 314.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 932702-07-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 340.6 °C at 760 mmHg
    3. Flash Point: 159.8 °C
    4. Appearance: /
    5. Density: 1.496
    6. Refractive Index: 1.621
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate(932702-07-3)
    11. EPA Substance Registry System: tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate(932702-07-3)
  • 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: 932702-07-3(Hazardous Substances Data)

932702-07-3 Usage

Uses

Used in Medicinal Chemistry and Drug Development:
Tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate is used as a building block for the synthesis of bioactive molecules, contributing to the development of new drugs and therapeutic agents.
Used in Antimicrobial and Antifungal Applications:
Due to its isothiazole ring system, tert-Butyl 6-bromobenzo[d]isothiazole-3-carboxylate has shown potential as an antimicrobial and antifungal agent, making it a valuable compound for the development of treatments against various infections.

Check Digit Verification of cas no

The CAS Registry Mumber 932702-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,2,7,0 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 932702-07:
(8*9)+(7*3)+(6*2)+(5*7)+(4*0)+(3*2)+(2*0)+(1*7)=153
153 % 10 = 3
So 932702-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H12BrNO2S/c1-12(2,3)16-11(15)10-8-5-4-7(13)6-9(8)17-14-10/h4-6H,1-3H3

932702-07-3SDS

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 tert-butyl 6-bromo-1,2-benzothiazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 6-bromo-1,2-benzoisothiazole-3-carboxylate

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:932702-07-3 SDS

932702-07-3Downstream Products

932702-07-3Relevant articles and documents

1 H-INDAZOLES, BENZOTHIAZOLES, 1,2-BENZOISOXAZOLES, 1,2-BENZOISOTHIAZOLES, AND CHROMONES AND PREPARATION AND USES THEREOF

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Page/Page column 69-70, (2010/11/27)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of -disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, pyrazolopyridines, isothiazolopyridines, and preparation and uses thereof

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Page/Page column 62, (2010/11/26)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nACh receptors), activation of nACh receptors, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (e.g., indazoles and benzothiazoles), which act as ligands for the α7 nACh receptor subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

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