17231-17-3 Usage
Uses
Used in Pharmaceutical Industry:
3,4-Dichlorothiophenol is used as a chemical intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Dye Industry:
3,4-DICHLOROTHIOPHENOL serves as a building block in the production of dyes, playing a crucial role in the creation of colorants for various applications.
Used in Pesticide Industry:
3,4-Dichlorothiophenol is utilized as an intermediate in the synthesis of pesticides, aiding in the development of agricultural chemicals to protect crops.
Used in Chemical Production:
Beyond its applications in specific industries, 3,4-Dichlorothiophenol is also used as a general building block in the production of a wide array of other chemicals, highlighting its versatility in the chemical sector.
Check Digit Verification of cas no
The CAS Registry Mumber 17231-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,3 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17231-17:
(7*1)+(6*7)+(5*2)+(4*3)+(3*1)+(2*1)+(1*7)=83
83 % 10 = 3
So 17231-17-3 is a valid CAS Registry Number.
17231-17-3Relevant articles and documents
Metal-free reductive cleavage of C-O σ-bonds in acyloin derivatives by an organic neutral super-electron-donor
Cutulic, Sylvain P. Y.,Findlay, Neil J.,Zhou, Sheng-Ze,Chrystal, Ewan J. T.,Murphy, John A.
supporting information; experimental part, p. 8713 - 8718 (2009/12/28)
(Chemical Equation Presented) Neutral organic electron-donor 7, formally a pyridinylidene carbene dimer, effects reductive cleavage of C-O σ-bonds in acyloin derivatives Ar(CO)CRR′OX (X = OAc, OPiv, OBz, OMs) and this represents the first cleavage of C-O σ-bonds by a neutral organic electron-donor. The methodology is applicable to a large array of substrates and the reduced counterparts were isolated in good to excellent yields. For certain substrates, donor 7 behaves as a base, effecting condensation reactions with some acetate ester derivatives of acyloins, leading to butenolides. The variation in reactivity among the different substrates was rationalized. 2009 American Chemical Society.
