1422007-52-0 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Fluoro-4,6-dihydro-thieno[3,4-b]thiophene-2-carboxylic acid methyl ester is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure and potential biological activity contribute to the development of new therapeutic agents for the treatment of different diseases.
Used in Agrochemical Synthesis:
In the agrochemical industry, 3-Fluoro-4,6-dihydro-thieno[3,4-b]thiophene-2-carboxylic acid methyl ester serves as a building block for the creation of novel agrochemicals. Its incorporation into these compounds can enhance their effectiveness in pest control and crop protection.
Used in Organic Compound Preparation:
3-Fluoro-4,6-dihydro-thieno[3,4-b]thiophene-2-carboxylic acid methyl ester is utilized as a versatile starting material in the preparation of other organic compounds. Its unique structural properties allow for the synthesis of a wide range of molecules with potential applications in various fields, including materials science, chemical research, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1422007-52-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,0,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1422007-52:
(9*1)+(8*4)+(7*2)+(6*2)+(5*0)+(4*0)+(3*7)+(2*5)+(1*2)=100
100 % 10 = 0
So 1422007-52-0 is a valid CAS Registry Number.
1422007-52-0Relevant academic research and scientific papers
Method of producing polythienothiophene
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Paragraph 0122-0124, (2017/11/03)
PROBLEM TO BE SOLVED: To provide a method of efficiently manufacturing a thienothiophene compound having an acyl group at a second position and a fluoro group at a third position. SOLUTION: This method of manufacturing a thienothiophene compound represented by formula (1) includes processes of: (a) obtaining a 3-fluorothiophene compound represented by formula (3) from a 3-aminothiophene compound represented by formula (2); (b) obtaining a dihydrothienothiophene compound represented by formula (4) from the 3-fluorothiophene compound represented by formula (3); and (c) obtaining the thienothiophene compound represented by formula (1) from the dihydrothienothiophene compound represented by formula (4). COPYRIGHT: (C)2013,JPOandINPIT
