6320-01-0 Usage
Description
3-Bromothiophenol is an organic compound that belongs to the class of thiophene derivatives. It is characterized by the presence of a bromine atom at the 3rd position and a thiol group, making it a valuable intermediate in the synthesis of various organic compounds. It appears as a clear, colorless to light yellow liquid.
Uses
Used in Chemical Synthesis:
3-Bromothiophenol is used as a key intermediate in the synthesis of various organic compounds, particularly those involving thiophene and its derivatives. Its unique structure allows for further functionalization and modification, making it a versatile building block in organic chemistry.
Used in Pharmaceutical Industry:
3-Bromothiophenol is used as a starting material for the development of new pharmaceutical compounds. Its ability to be functionalized with sulfonium groups and other moieties makes it a promising candidate for the creation of novel drugs with potential therapeutic applications.
Used in Material Science:
3-Bromothiophenol can be used in the development of functional materials, such as those with specific electronic, optical, or magnetic properties. Its versatility in chemical synthesis allows for the creation of materials with tailored properties for various applications, including sensors, energy storage, and electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 6320-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6320-01:
(6*6)+(5*3)+(4*2)+(3*0)+(2*0)+(1*1)=60
60 % 10 = 0
So 6320-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrS/c7-5-2-1-3-6(8)4-5/h1-4,8H/p-1
6320-01-0Relevant articles and documents
Oxidative cleavage of S-Arylmercaptoacetic acids by pyridinium chlorochromate: Kinetic and correlation analysis
Kabilan,Girija,Rajagopal
, p. 683 - 688 (2007/10/03)
Kinetics of oxidation of 24 S-Arylmercaptoacetic acids (SAMA) by pyridinium chlorochromate (PCC) 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 well with σI, σ°R values and the meta-compounds correlate well with F,R values. The reaction constants are negative and of smaller magnitudes. Further, the ortho-substituted acids show a good correlation with triparametric equation involving Taft's σI and σ°R and charton's steric parameter v. There is no considerable steric contribution to the total orthosubstituent effect. Based on these observations, the mechanism involving the formation of protonated arylsulfinylacetic acid intermediate, followed by an intramolecular rearrangement leading to the product thiophenol has been proposed.
S-Aryl(tetramethyl)isothiouronium salts as potential antimicrobial agents, II
Tait,Parenti,Di Bella,Bondi,Quaglio
, p. 203 - 210 (2007/10/02)
-
