39165-62-3

Basic information

• Product Name: Propanesulfinicacid,sodiumsalt
• Synonyms: Propanesulfinicacid,sodiumsalt
• CAS NO: 39165-62-3
• Molecular Formula: C₃H₇O₂S*Na
• Molecular Weight: 130.14125
• Mol File: 39165-62-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Propanesulfinicacid,sodiumsalt(CAS DataBase Reference)
• NIST Chemistry Reference: Propanesulfinicacid,sodiumsalt(39165-62-3)
• EPA Substance Registry System: Propanesulfinicacid,sodiumsalt(39165-62-3)

Safety Data

• Hazardous Substances Data: 39165-62-3(Hazardous Substances Data)

Upstream product

• 10147-36-1 n-propanesulfonyl chloride 
• 144-55-8 sodium hydrogencarbonate 
• 7757-83-7 sodium sulfite 
• 6898-84-6 sodium 1-propanethiolate 

Downstream Products

• 84264-88-0 4-(propane-1-sulfonyl)-benzaldehyde 
• 1571134-83-2 1-[4-cyano-2-(propane-1-sulfonyl)benzyl]-6-methyl-4-oxo-5-(3-(trifluoromethyl)phenyl)-1,4-dihydropyridine-3-carboxylic acid methylamide 
• 1132842-77-3 4-Methyl-5-[(propylsulfonyl)(2,3,6-trifluorophenyl)methyl]pyridine-2-carboxamide 
• 50366-59-1 1-(4-Bromo-phenyl)-3-(propane-1-sulfonyl)-propan-1-one 
• 50366-58-0 1-Phenyl-3-(propane-1-sulfonyl)-propan-1-one 
• 39165-57-6 cyclohexyl propane-1-thiosulfonate 
• 123151-23-5 diphenylmethyl 7β-<2-<2-<<(tert-butyloxy)carbonyl>amino>thiazol-4-yl>-2(Z)-(methoxyimino)acetamido>-3-(1-propylsulfonyl)-1-carba-1-dethia-3-cephem-4-carboxylate 
• 82465-85-8 2-Benzamido-2-propansulfonylmethyl-1,1,1-trichlorethan 
• 82465-86-9 2-Phenylacetamido-2-propansulfonylmethyl-1,1,1-trichlorethan 

Relevant articles and documents

PYRIDYL OR PYRIMIDYL MTOR KINASE INHIBITORS

The invention relates to compounds or pharmaceutically acceptable salts thereof of formula (I): (I) wherein R1, R2, R3, R4, R4' and R5 are as defined in the description and claims; and comp

Eosin Y (EY) Photoredox-Catalyzed Sulfonylation of Alkenes: Scope and Mechanism

Alkyl- and aryl vinyl sulfones were obtained by eosin Y (EY)-mediated visible-light photooxidation of sulfinate salts and the reaction of the resulting S-centered radicals with alkenes. Optimized reaction conditions, the sulfinate and alkene scope, and X-ray structural analyses of several reaction products are provided. A detailed spectroscopic study explains the reaction mechanism, which proceeds through the EY radical cation as key intermediate oxidizing the sulfinate salts.

CONVERSIONS OF MERCAPTANS DURING CATALYTIC OXIDATION BY MOLECULAR OXYGEN IN AQUEOUS ALKALINE SOLUTIONS

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