2557-78-0 Usage
Description
2-Fluorothiophenol is an organic compound characterized by a clear colorless to light yellow liquid appearance. It is composed of a thiophenol group with a fluorine atom at the 2nd position, which imparts unique chemical properties to the molecule.
Uses
Used in Chemical Synthesis:
2-Fluorothiophenol is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to be a versatile building block in the synthesis of complex molecules.
2-Fluorothiophenol is used as a synthetic intermediate for [application reason] in the chemical synthesis industry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Fluorothiophenol may be utilized as a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors. Its unique chemical properties can be exploited to design molecules with enhanced potency and selectivity.
2-Fluorothiophenol is used as a key component in [application reason] for the pharmaceutical industry.
Used in Material Science:
The distinct properties of 2-Fluorothiophenol can also make it a valuable additive or component in the development of new materials with specific characteristics, such as improved stability, reactivity, or conductivity.
2-Fluorothiophenol is used as an additive/component for [application reason] in the material science industry.
Check Digit Verification of cas no
The CAS Registry Mumber 2557-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2557-78:
(6*2)+(5*5)+(4*5)+(3*7)+(2*7)+(1*8)=100
100 % 10 = 0
So 2557-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H5FS/c7-5-3-1-2-4-6(5)8/h1-4,8H/p-1
2557-78-0Relevant articles and documents
Sulphonamide derivatives
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, (2008/06/13)
The present invention relates to the potentiation of glutamate receptor function using certain sulphonamide derivatives. It also relates to novel sulphonamide derivatives, to processes for their preparation and to pharmaceutical compositions containing them.
Oxidative Cleavage of S-Arylmercaptoacetic Acids by Sodium Perborate: Kinetic and Correlation Study
Kabilan, S.,Pandiarajan, K.,Krishnasamy, K.,Sankar, P.
, p. 443 - 452 (2007/10/02)
Kinetics of oxidation of twenty six S-arylmercaptoacetic acids (SAMA) (I) by sodium perborate (PB) have been studied in acid medium.The product of oxidation is the corresponding thiophenol.The rate data of meta- and para-substituted acids have been correlated with DSP equations.While the para-compounds correlate well with ?I and ?0R values, the meta-compounds correlate well with ?I and ?-R values.The reaction constants are negative and of smaller magnitudes.Further, the ortho-substituted acids show a good correlation with a triparametric equation involving Taft's ?I and ?0R and Charton's steric parameter ν.There is a considerable steric contribution to the total ortho-substituent effect.Based on these observations, mechanism involving the formation of protonated arylsulfinylacetic acid intermediate, followed by an intramolecular rearrangement leading to the product thiophenol has been proposed.
Fluorinated neuroleptics of the 10-piperazino-10,11-dihydrodibenzo[b,f]thiepin series; 6-Fluoro derivatives of perathiepin, octoclothepin, doclothepin and some related compounds
Cervena,Metysova,Bartl,Protiva
, p. 2139 - 2155 (2007/10/05)
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