76151-64-9 Usage
### Properties
1. Molecular Formula: C14H10ClNO2S2
2. Type: Organic compound
3. Core Structure: Benzothiazole
4. Functional Groups:
Sulfonyl Chloride Group
Chlorobenzene Substituent
### Applications
1. Synthesis:
Intermediate in the synthesis of pharmaceuticals
Intermediate in the synthesis of agrochemicals
2. Potential Uses:
Materials Science
Chemical Research
### Significance
1. Valuable Building Block:
Its structural properties and reactivity make it valuable.
Used for creating new molecules with potential properties.
Potential applications in scientific and industrial fields.
Versatile
Offers versatility in chemical synthesis.
Role
Fundamental in designing new compounds.
Potential Impact
Enhances possibilities in pharmaceuticals and agrochemicals.
Utility
Useful for creating specialized materials in materials science.
This compound's characteristics and applications make it a versatile and important component in various scientific and industrial processes, ranging from pharmaceuticals to materials science and chemical research. Its role as an intermediate adds to its significance in the creation of new compounds with desired properties.
Check Digit Verification of cas no
The CAS Registry Mumber 76151-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,5 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76151-64:
(7*7)+(6*6)+(5*1)+(4*5)+(3*1)+(2*6)+(1*4)=129
129 % 10 = 9
So 76151-64-9 is a valid CAS Registry Number.
76151-64-9Relevant articles and documents
Novel aromatic fluoroolefins via fluoro-Julia-Kocienski olefination
Allendoerfer, Nadine,Es-Sayed, Mazen,Nieger, Martin,Braese, Stefan
experimental part, p. 3439 - 3448 (2010/12/19)
Fluoroolefins, which play an increasingly important role as peptide mimics in pharmaceuticals and as crop protection agents, are generated using a fluoro-Julia-Kocienski olefination. Their preparation can easily be accomplished using a Mitsunobu reaction and subsequent oxidation to generate the required benzothiazolyl sulfones. The key step of this process was the electrophilic -fluorination of the sulfone with N-fluorobenzenesulfonimide. The last stage of the successful synthesis of the fluoroolefins was the modified Julia-Kocienski olefination under basic conditions. Further functionalization was followed with the application of a Suzuki reaction. Georg Thieme Verlag Stuttgart.
