343229-18-5

Basic information

• Product Name: 4-methyl-N'-(3-fluorobenzylidene)benzenesulfonohydrazide
• Synonyms: 4-methyl-N'-(3-fluorobenzylidene)benzenesulfonohydrazide
• CAS NO: 343229-18-5
• Molecular Weight: 292.334
• Mol File: 343229-18-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-methyl-N'-(3-fluorobenzylidene)benzenesulfonohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N'-(3-fluorobenzylidene)benzenesulfonohydrazide(343229-18-5)
• EPA Substance Registry System: 4-methyl-N'-(3-fluorobenzylidene)benzenesulfonohydrazide(343229-18-5)

Safety Data

• Hazardous Substances Data: 343229-18-5(Hazardous Substances Data)

Upstream product

• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 456-48-4 3-Fluorobenzaldehyde 

Downstream Products

• 149739-61-7 3-(3-fluorophenyl)-1H-pyrazole 
• 501-00-8 3-fluorophenylacetonitrile 
• 127974-67-8 1--3-fluorobenzene 
• 187343-51-7 3-(3-fluorophenyl)-5-phenyl-1H-pyrazole 
• 73900-35-3 1-((1S,2R,3S)-2,3-Dimethyl-cyclopropyl)-3-fluoro-benzene 
• 73925-92-5 1-((1R,2S,3R)-2,3-Dimethyl-cyclopropyl)-3-fluoro-benzene 
• 73900-35-3 1-((2R,3R)-2,3-Dimethyl-cyclopropyl)-3-fluoro-benzene 
• 73900-31-9 1-Fluoro-3-(2-methyl-but-3-enyl)-benzene 
• 65354-65-6 2-(m-Fluorophenyl)-3,3-dimethylmethylenecyclopropane 
• 65354-71-4 2-(m-Fluorophenyl)isopropylidenecyclopropane 
• 73900-15-9 m-fluorophenyldiazomethane 

Relevant articles and documents

Regioselectivity in the Addition of Singlet and Triplet Carbenes to 1,1-Dimethylallene. A Probe for Carbene Multiplicity

Singlet carbenes add preferentially to the more substituted bond of 1,1-dimethylallene (1), to give methylenecyclopropanes 3 as the major product.In contrast, many triplet carbenes add with differing regioselectivity, giving the thermodynamically preferre

Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones

A domino process that converges the migratory insertion of carbene with a Heck reaction has been established as a versatile tool for the synthesis of 2-arylidene-3-aryl-1-indanones from very stable and easily accessible N-tosylhydrazones and 2′-iodochalco