42381-27-1 Usage
Description
4-Hydrazino-N-methylbenzeneethanesulfonamide hydrochloride is an organic compound that serves as an intermediate in the synthesis of various pharmaceuticals. It is a yellow to light yellow crystalline powder, which is a characteristic of its chemical properties.
Uses
Used in Pharmaceutical Industry:
4-Hydrazino-N-methylbenzeneethanesulfonamide hydrochloride is used as an intermediate in the preparation of the antimigraine drug Naratriptan (N378730). It plays a crucial role in the synthesis process, contributing to the development of medications that help alleviate migraine symptoms and improve the quality of life for patients suffering from this condition.
As a Naratriptan intermediate, 4-Hydrazino-N-methylbenzeneethanesulfonamide hydrochloride is essential in the pharmaceutical industry for the production of effective treatments for migraines. Its chemical properties and structure make it a valuable component in the synthesis of Naratriptan, which is a selective serotonin agonist that works by narrowing blood vessels in the brain and reducing the release of substances that cause inflammation, pain, and other migraine symptoms.
Check Digit Verification of cas no
The CAS Registry Mumber 42381-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,8 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42381-27:
(7*4)+(6*2)+(5*3)+(4*8)+(3*1)+(2*2)+(1*7)=101
101 % 10 = 1
So 42381-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H15N3O2S.ClH/c1-11-15(13,14)7-6-8-2-4-9(12-10)5-3-8;/h2-5,11-12H,6-7,10H2,1H3;1H
42381-27-1Relevant articles and documents
Synthesis of n-methyl benzenemethane sulfonamide substituted carbazoles and pyrazoles
Rao, B. Venugopala,Hariharakrishnan,Dubey
scheme or table, p. 1191 - 1194 (2012/08/07)
Cyclization of 1-(4-hydrazinophenyl)-N-methylmethanesulfonamide hydrochloride (2) with cyclohexanone (3)/N-methyl-4-piperidone (5) afforded the corresponding N-methyl-1-(2,3,4,9-tetrahydro-1H-carbazol-6-yl)methanesulfonamide (4) and N-methyl-1-(2-methyl- 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-8-yl) methane sulfonamide (6). Condensation of compound 2 with substituted aryl β-diketones gave the novel N-methyl-1-[4-(3-methyl-5-phenyl-1H-pyrazol-1- yl)phenyl]methanesulfonamide (8). All the synthesized compounds were characterized by their FT-IR, 1H NMR and mass spectral data.