68326-56-7

Basic information

• Product Name: (R)-1-[(4-methylphenyl)sulfinyl]butan-2-one
• Synonyms: (R)-1-[(4-methylphenyl)sulfinyl]butan-2-one
• CAS NO: 68326-56-7
• Molecular Weight: 210.297
• Mol File: 68326-56-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (R)-1-[(4-methylphenyl)sulfinyl]butan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-[(4-methylphenyl)sulfinyl]butan-2-one(68326-56-7)
• EPA Substance Registry System: (R)-1-[(4-methylphenyl)sulfinyl]butan-2-one(68326-56-7)

Safety Data

• Hazardous Substances Data: 68326-56-7(Hazardous Substances Data)

Upstream product

• 1517-82-4 (1R,2S,5R,SS)-(-)-menthyl p-toluenesulfinate 
• 1519-39-7 (R)-methyl p-tolyl sulfoxide 
• 107-12-0 propiononitrile 
• 29066-36-2 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl propionate 
• 105-37-3 Ethyl propionate 
• 83859-14-7 N,N-Dimethyl-N'-[1-((R)-toluene-4-sulfinylmethyl)-prop-(E)-ylidene]-hydrazine 

Downstream Products

• 136347-14-3 (S)-2-hydroxy-2-<<(4-methylphenyl)sulfenyl>methyl>butanamide 
• 71925-83-2 (R,Rs)-1-(4-methylphenylsulfinyl)-2-butanol 
• 71899-72-4 (2S,R_S)-1-(p-tolylsulfinyl)butan-2-ol 
• 136347-10-9 (S₂,R_S)-2-hydroxy-2-<<(4-methylphenyl)sulfinyl>methyl>butanenitrile 
• 136347-12-1 (R)-2-Hydroxy-2-((R)-toluene-4-sulfinylmethyl)-butyronitrile 

Relevant articles and documents

Highly enantiomeric purity conversion of α-sulfinyl oximes and α-sulfinyl hydrazones to the corresponding β-keto sulfoxides with butyltriphenylphosphonium periodate (BUTPPPI)

Butyltriphenylphosphonium periodate (Ph3P+BuIO 4-)1 is readily prepared as a white solid from butyltriphenylphosphonium chloride, performs conversion of α-sulfinyl oximes (2) and α-sulfinyl hydrazones (4) to the

Highly Diastereoselective Hydrocyanation of β-Keto Sulfoxides: Synthesis of Enantiomerically Pure Cyanohydrin Derivatives

The reactions of chiral β-keto sulfoxides, R1-CO-CHR2-SOTol (R1 = Me, n-Pr, i-Pr, t-Bu, Ph; R2 = H, Me) with Et2AlCN yield the corresponding sulfinyl cyanohydrins with high yields (85-96percent) and de (>96perce

Stereospecific Synthesis of Chiral α-Sulfinylhydrazones

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