1239370-98-9 Usage
Uses
Used in Pharmaceutical Industry:
Potassium (5-bromothiophen-2-yl)trifluoroboranuide is used as a reagent in the synthesis of various pharmaceutical compounds. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it a valuable component in the development of new drugs and medications.
Used in Agrochemical Production:
In the agrochemical industry, Potassium (5-bromothiophen-2-yl)trifluoroboranuide is utilized as a reagent for the synthesis of various agrochemicals. Its role in forming essential chemical bonds contributes to the production of effective and efficient agrochemicals for agricultural applications.
Used in Specialty Chemicals Manufacturing:
Potassium (5-bromothiophen-2-yl)trifluoroboranuide is also used in the production of specialty chemicals, where its unique properties and reactivity are leveraged to create specific chemical compounds for various applications.
Used as a Catalyst in Chemical Reactions:
Due to its reactivity and ability to form various chemical bonds, Potassium (5-bromothiophen-2-yl)trifluoroboranuide can also be used as a catalyst in different chemical reactions. This enhances the efficiency and selectivity of the reactions, making it a valuable tool in chemical research and manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 1239370-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,3,7 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1239370-98:
(9*1)+(8*2)+(7*3)+(6*9)+(5*3)+(4*7)+(3*0)+(2*9)+(1*8)=169
169 % 10 = 9
So 1239370-98-9 is a valid CAS Registry Number.
1239370-98-9Relevant academic research and scientific papers
Preparation of brominated 2-alkoxythiophenes via oxidation and etherification of 2-thienyltrifluoroborate salts
Tietz, Jonathan I.,Seed, Alexander J.,Sampson, Paul
supporting information, p. 5058 - 5061 (2013/01/15)
The synthesis of ring brominated long-chain 2-alkoxythiophenes is reported, involving mild (Oxone) oxidation of readily prepared 2-thienyltrifluoroborate salts followed by Mitsunobu etherification. Both procedures are operationally straightforward and use inexpensive reagents. Using this approach, several novel mono- and dibrominated octyloxythiophenes with previously elusive substitution patterns were prepared. One such compound was elaborated to a novel 5-alkoxythieno[3,2-b]thiophene-2-carboxylate ester, marking the first synthetic entry into this family of compounds.
