21309-15-9

Basic information

• Product Name: Benzene, [[(1R,2S)-2-phenylcyclopropyl]sulfonyl]-, rel-
• CAS NO: 21309-15-9
• Molecular Formula: C15H14O2S
• Molecular Weight: 258.341
• Mol File: 21309-15-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, [[(1R,2S)-2-phenylcyclopropyl]sulfonyl]-, rel-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [[(1R,2S)-2-phenylcyclopropyl]sulfonyl]-, rel-(21309-15-9)
• EPA Substance Registry System: Benzene, [[(1R,2S)-2-phenylcyclopropyl]sulfonyl]-, rel-(21309-15-9)

Safety Data

• Hazardous Substances Data: 21309-15-9(Hazardous Substances Data)

Upstream product

• 28187-87-3 (E)-((3-bromoprop-1-en-1-yl)sulfonyl)benzene 
• 16212-06-9 phenyl styryl sulfone 
• 1774-47-6 trimethylsulfoxonium iodide 
• 873-55-2 sodium benzenesulfonate 
• 1228297-54-8 3-chloro-3-phenyl-propyl phenyl sulfone 
• 104-87-0 4-methyl-benzaldehyde 
• 104-88-1 4-chlorobenzaldehyde 
• 100-52-7 benzaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 630-19-3 pivalaldehyde 
• 104-55-2 3-phenyl-propenal 
• 58688-13-4 cis-2-phenyl-1-(phenylthio)cyclopropane 
• 100-42-5 styrene 
• 7205-91-6 phenylthiomethyl chloride 

Relevant articles and documents

Synthesis of substituted tetrahydrofurans via intermolecular reactions of γ-chlorocarbanions of 3-substituted 3-chloro-propylphenyl sulfones with aldehydes

Carbanions of 3-substituted-3-chloropropyl phenyl sulfones add to carbonyl groups of aldehydes to produce aldol type adducts that undergo 1,5-intramolecular substitution giving 2,3,5-trisubstituted tetrahydrofurans. The effect of substituents in the 3-pos

Reactivity of bifunctional olefins with hydrazine hydrate - Part II

The reaction of 1-aroyl-2-arylsulfonylethenes 1 with different ratios of hydrazine hydrate lead to hydrazones, dimerized products and 2-pyrazolines. The reactivity of pyrazolines has also been studied by dehydrogenation, pyrolysis, nitrosation and acylation.