80775-39-9 Usage
Uses
Used in Pharmaceutical Industry:
3-Acetyl-2,5-dibromothiophene is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical properties and reactivity. It contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Acetyl-2,5-dibromothiophene is utilized as a building block in the creation of novel agrochemicals, such as pesticides and herbicides, due to its ability to enhance the effectiveness and selectivity of these compounds.
Used in Flavoring Agent for Food Industry:
3-Acetyl-2,5-dibromothiophene is used as a flavoring agent in the food industry, capitalizing on its strong odor to impart unique and desirable flavors to various food products.
Used in Organic Synthesis:
3-Acetyl-2,5-dibromothiophene serves as a versatile building block in organic synthesis, enabling the creation of a wide range of organic compounds with diverse applications in various industries.
Used in Material Science:
In the field of material science, 3-Acetyl-2,5-dibromothiophene is employed in the development of new materials with specific properties, such as improved thermal stability, electrical conductivity, or chemical resistance, contributing to advancements in various technological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 80775-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,7 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80775-39:
(7*8)+(6*0)+(5*7)+(4*7)+(3*5)+(2*3)+(1*9)=149
149 % 10 = 9
So 80775-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Br2OS/c1-3(9)4-2-5(7)10-6(4)8/h2H,1H3
80775-39-9Relevant academic research and scientific papers
Bromothiophene Reactions. I. Friedel-Crafts Acylation
Agua, M. J. del,Alvarez-Insua, A. S.,Conde, S.
, p. 1345 - 1347 (2007/10/02)
Friedel-Crafts acylation of 2,5-dibromo- and 2,3,5-tribromothiophenes with different acyl chlorides and anhydrous aluminium trichloride has been studied.The reaction afforded a mixture of acyl derivatives and tetrabromothiophene.The results obtained suggest a mechanism which involves the formation of bromine cations in the reaction medium.Several products obtained in this reaction are described.
