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4-Bromobenzo[d]thiazole-2-thiol is a chemical compound characterized by the molecular formula C7H4BrNS2. It is a thiazole derivative featuring a bromine substituent and a thiol group attached to the benzene ring. This yellowish to brown solid is primarily utilized in organic synthesis and pharmaceutical research, offering unique chemical structure and properties that make it a promising candidate for drug development and other pharmaceutical applications.

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  • 1083181-41-2 Structure
  • Basic information

    1. Product Name: 4-Bromobenzo[d]thiazole-2-thiol
    2. Synonyms: 4-Bromobenzo[d]thiazole-2-thiol;4-BroMobenzothiazole-2-thiol
    3. CAS NO:1083181-41-2
    4. Molecular Formula: C7H4BrNS2
    5. Molecular Weight: 246.14736
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1083181-41-2.mol
  • Chemical Properties

    1. Melting Point: 184-185 °C
    2. Boiling Point: 350.6±44.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.93±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 8.68±0.20(Predicted)
    10. CAS DataBase Reference: 4-Bromobenzo[d]thiazole-2-thiol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-Bromobenzo[d]thiazole-2-thiol(1083181-41-2)
    12. EPA Substance Registry System: 4-Bromobenzo[d]thiazole-2-thiol(1083181-41-2)
  • 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: 1083181-41-2(Hazardous Substances Data)

1083181-41-2 Usage

Uses

Used in Pharmaceutical Research and Development:
4-Bromobenzo[d]thiazole-2-thiol is used as a key intermediate in the synthesis of various pharmaceuticals for its potential role in the development of new drugs. Its unique chemical structure allows it to be a building block in creating novel compounds with therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 4-Bromobenzo[d]thiazole-2-thiol serves as a valuable precursor for the creation of a wide range of organic compounds and materials. Its reactivity and functional groups make it suitable for various synthetic pathways, contributing to the advancement of chemical research and the production of new materials.
Used in Research Applications:
4-Bromobenzo[d]thiazole-2-thiol is employed in research settings to explore its chemical properties and potential interactions with other molecules. This helps in understanding its behavior and applicability in different chemical and biological contexts, further expanding its utility in scientific investigations.
Overall, 4-Bromobenzo[d]thiazole-2-thiol's applications span across pharmaceutical research, organic synthesis, and broader research applications, highlighting its versatility and importance in the scientific and industrial sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 1083181-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,3,1,8 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1083181-41:
(9*1)+(8*0)+(7*8)+(6*3)+(5*1)+(4*8)+(3*1)+(2*4)+(1*1)=132
132 % 10 = 2
So 1083181-41-2 is a valid CAS Registry Number.

1083181-41-2SDS

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 4-Bromo-2-mercaptobenzothiazole

1.2 Other means of identification

Product number -
Other names 4-bromo-3H-1,3-benzothiazole-2-thione

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:1083181-41-2 SDS

1083181-41-2Downstream Products

1083181-41-2Relevant articles and documents

Synthesis of 2-mercaptobenzothiazoles via DBU-promoted tandem reaction of o-haloanilines and carbon disulfide

Wang, Fei,Cai, Shangjun,Wang, Zhipeng,Xi, Chanjuan

, p. 3202 - 3205 (2011)

An efficient strategy for the synthesis of a variety of 2-mercaptobenzothiazole derivatives has been developed. The reaction proceeded from o-haloaniline derivatives and carbon disulfide via a tandem reaction in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) to afford the corresponding 2-mercaptobenzothiazole derivatives in good to excellent yields.

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