86810-78-8 Usage
Description
4-(propylsulfonyl)aniline is a chemical compound with the molecular formula C9H13NO2S. It is a white to light yellow crystalline solid that serves as an intermediate in the synthesis of pharmaceuticals and other organic compounds.
Uses
Used in Pharmaceutical Industry:
4-(propylsulfonyl)aniline is used as an intermediate in the synthesis of pharmaceuticals for its ability to bond with other compounds and create complex molecules, contributing to the development of new drugs.
Used in Dye and Pigment Industry:
4-(propylsulfonyl)aniline is used as a precursor in the production of dyes and pigments due to its chemical properties that allow for the creation of a variety of colorants.
Used in Plastics and Polymer Industry:
4-(propylsulfonyl)aniline is utilized in the production of various types of plastics and polymers, where its bonding capabilities enhance the formation of complex and useful materials.
Safety Note:
4-(propylsulfonyl)aniline is considered to be a hazardous substance and should be handled with care, adhering to proper safety protocols to ensure the protection of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 86810-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,1 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86810-78:
(7*8)+(6*6)+(5*8)+(4*1)+(3*0)+(2*7)+(1*8)=158
158 % 10 = 8
So 86810-78-8 is a valid CAS Registry Number.
86810-78-8Relevant articles and documents
Syntheses of Some Alkyl-, Cycloalkyl-, and Aryl-(4-aminophenyl)-sulfones
Courtin, Alfred
, p. 1046 - 1052 (2007/10/02)
Syntheses of (4-aminophenyl)-alkyl, -cycloalkyl and -aryl sulfones 2 were achieved both by alkylation of 4-(acetylamino)-benzenesulfinic acid (7) to the corresponding acetanilides 9 followed by hydrolysis and by oxidation of the appropriate (4-nitrophenyl)-sulfides 11 to (4-nitrophenyl)-sulfones 1 with subsequent Bechamp reduction.
