395664-58-1 Usage
General Description
2-Thiophenecarboxylic acid, 4,5-dibromo-3-fluoro-, methyl ester is a chemical compound with the molecular formula C8H5Br2FO2S. It is an ester formed from the reaction of 2-thiophenecarboxylic acid with methyl alcohol. This chemical is a derivative of thiophene, a heterocyclic compound found in various natural products and pharmaceuticals. The presence of bromine and fluorine atoms in the molecule makes it potentially useful in pharmaceutical and agrochemical industries for the development of new compounds with specific biological activities. It is important to handle this chemical with care and follow proper safety precautions due to its potential toxicity and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 395664-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,5,6,6 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 395664-58:
(8*3)+(7*9)+(6*5)+(5*6)+(4*6)+(3*4)+(2*5)+(1*8)=201
201 % 10 = 1
So 395664-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Br2FO2S/c1-11-6(10)4-3(9)2(7)5(8)12-4/h1H3
395664-58-1Relevant articles and documents
NOVEL HETEROCYCLIC COMPOUNDS AS BET INHIBITORS
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Page/Page column 81-82, (2022/01/24)
Provided are heterocyclic compounds of formula (I) as bromodomain and extraterminal (BET) inhibitors, pharmaceutical compositions comprising the compounds, their synthesis and their use for treating diseases and conditions wherein inhibition of one or more BET bromodomains provides a benefit.
Ring fluorinated thiophenes: Applications to liquid crystal synthesis
Kiryanov, Andre A.,Seed, Alexander J.,Sampson, Paul
, p. 8797 - 8800 (2007/10/03)
Ring fluorinated thiophenes were synthesized via a Balz-Schiemann fluorination approach and were successfully employed in the synthesis of liquid crystals using regioselective electrophilic bromination and regioselective Suzuki coupling chemistry.
