6387-28-6 Usage
Description
(4-aminophenyl)methanesulfonic acid, also known as methanesulfonic acid p-aminophenyl ester, is a compound with the chemical formula C7H9NO3S. It is a white to off-white crystalline powder that exhibits versatile chemical properties, making it a valuable reagent in various fields.
Uses
Used in Pharmaceutical and Agrochemical Industries:
(4-aminophenyl)methanesulfonic acid is used as a reagent in the synthesis of various pharmaceuticals and agrochemicals due to its ability to facilitate the creation of complex molecules.
Used in Chemical Synthesis:
As a sulfonamide derivative, (4-aminophenyl)methanesulfonic acid is used in the synthesis of a wide range of drugs and dyes, contributing to the diversity of products in these markets.
Used in Photography:
(4-aminophenyl)methanesulfonic acid is used as a stabilizer for metal salts in photographic developing solutions, ensuring the stability and quality of the developed images.
Used in Biochemical and Molecular Biology Research:
(4-aminophenyl)methanesulfonic acid is also employed as a buffer in biochemical and molecular biology research, helping to maintain optimal conditions for various biological reactions and analyses.
Check Digit Verification of cas no
The CAS Registry Mumber 6387-28-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,8 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6387-28:
(6*6)+(5*3)+(4*8)+(3*7)+(2*2)+(1*8)=116
116 % 10 = 6
So 6387-28-6 is a valid CAS Registry Number.
6387-28-6Relevant articles and documents
Examination of mercaptobenzyl sulfonates as catalysts for native chemical ligation: Application to the assembly of a glycosylated Glucagon-Like Peptide 1 (GLP-1) analogue
Cowper, Ben,Sze, Tsz Mei,Premdjee, Bhavesh,Bongat White, Aileen F.,Hacking, Andrew,Macmillan, Derek
supporting information, p. 3208 - 3210 (2015/06/30)
3/4-Mercaptobenzyl sulfonates were investigated as aryl thiol catalysts for native chemical ligation (NCL). Whilst catalysing NCL processes at a similar rate to 4-mercaptophenyl acetic acid (MPAA), the increased polarity and solubility of 3-mercaptobenzyl
Synthesis of 5-substituted indole derivatives. Part 3: A facile synthesis of 5-chloromethyl-1H-indole-2-carboxylates: Replacement of sulfonic acid functionality by chlorine
Pete, Béla,Toke, László
, p. 3373 - 3375 (2007/10/03)
Valuable new synthetic intermediates, 5-chloromethyl-1H-indole-2-carboxylates, were prepared by the elimination of SO2 from 2-ethoxycarbonyl-1H-indole-5-methanesulfonic acids, which are easily accessible by Fischer-type indolization.