20035-14-7

Basic information

• Product Name: S-(naphthalene-2-yl) naphthalene-2-sulfonothioate
• Synonyms: S-(naphthalene-2-yl) naphthalene-2-sulfonothioate
• CAS NO: 20035-14-7
• Molecular Weight: 350.462
• Mol File: 20035-14-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: S-(naphthalene-2-yl) naphthalene-2-sulfonothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(naphthalene-2-yl) naphthalene-2-sulfonothioate(20035-14-7)
• EPA Substance Registry System: S-(naphthalene-2-yl) naphthalene-2-sulfonothioate(20035-14-7)

Safety Data

• Hazardous Substances Data: 20035-14-7(Hazardous Substances Data)

Upstream product

• 96-09-3 styrene oxide 
• 10151-46-9 2-naphthylsulfonyl hydrazide 
• 95323-21-0 methyl naphthalene-2-sulfinate 
• 7732-18-5 water 
• 1950-79-4 naphthalene-2-sulfonyl iodide 
• 613-49-0 naphthalene-2-sulfinic acid 
• 201036-12-6 2-(benzylsulfinyl)naphthalene 

Relevant articles and documents

H4SiW12O40-catalyzed cyclization of epoxides/aldehydes and sulfonyl hydrazides: An efficient synthesis of 3,4-disubstituted 1H-pyrazoles

A simple and efficient method for the synthesis of pyrazoles through a silicotungstic acid (H4SiW12O40)-catalyzed cyclization of epoxides/aldehydes and sulfonyl hydrazides has been developed. Various epoxides/aldehydes were smoothly reacted with sulfonyl hydrazides to furnish regioselectivity 3,4-disubstituted 1H-pyrazoles. The application of such an earth-abundant, readily accessible, and nontoxic catalyst provides a green approach for the construction of 3,4-disubstituted 1H-pyrazoles. A plausible reaction mechanism has been proposed on the basis of control experiments, GC-MS and DFT calculations.