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.
1083181-41-2Relevant 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.