93921-42-7

Basic information

• Product Name: (+)-(2S,4R)-trans-2,4-dimethyl-1-cyclohexanone
• Synonyms: (+)-(2S,4R)-trans-2,4-dimethyl-1-cyclohexanone
• CAS NO: 93921-42-7
• Molecular Weight: 126.199
• Mol File: 93921-42-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (+)-(2S,4R)-trans-2,4-dimethyl-1-cyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(2S,4R)-trans-2,4-dimethyl-1-cyclohexanone(93921-42-7)
• EPA Substance Registry System: (+)-(2S,4R)-trans-2,4-dimethyl-1-cyclohexanone(93921-42-7)

Safety Data

• Hazardous Substances Data: 93921-42-7(Hazardous Substances Data)

Upstream product

• 23713-65-7 2,4-dimethylcyclohexan-1-ol 
• 78-79-5 isoprene 
• 105-67-9 2,4-Xylenol 
• 109068-24-8 (+/-)-3,5-dinitro-benzoic acid-(2t,4t-dimethyl-cyclohex-r-yl ester) 
• 23713-65-7 (+/-)-t-2,t-4-Dimethyl-1-r-cyclohexanol 
• 23713-65-7 (-)(1S,2S,4S)-2,4-Dimethyl-1-cyclohexanol 
• 53898-13-8 1-Methylen-2β.4β-dimethyl-cyclohexan 
• 82416-28-2 Acetate of (+/-)-2,4-Dimethyl-1-cyclohexanol 
• 66-81-9 Cycloheximide 
• 111003-03-3 c-2,t-4-Dimethyl-r-1-cyclohexanol 

Downstream Products

• 146098-89-7 (E,2R,4R)-(2,4-dimethylcyclohexane)benzylidene 
• 23713-65-7 (+/-)-t-2,t-4-Dimethyl-1-r-cyclohexanol 
• 23713-65-7 (+/-)-c-2,c-4-Dimethyl-1-r-cyclohexanol 
• 146098-93-3 (1R,2S,4S)-1-[(R)-((3aR,7aR)-1,3-Dimethyl-2-oxo-octahydro-2λ⁵-benzo[1,3,2]diazaphosphol-2-yl)-phenyl-methyl]-2,4-dimethyl-cyclohexanol 
• 69256-18-4 (-)-(2R,4R)-cis-2,4-Dimethyl-1-cyclohexanone 
• 6746-42-5 (+)-(2R,4S,6R,αR)-Isocycloheximide 
• 113776-10-6 (+)-(1S,2R,4R)-2,4-dimethylcyclohexanol 
• 111003-03-3 c-2,t-4-Dimethyl-r-1-cyclohexanol 
• 66-81-9 Cycloheximide 
• 642-81-9 Cycloheximide 
• 66-81-9 (2S,4S,6S,αS)-cycloheximide 
• 94130-63-9 (2S,4S,6R,αS)-cycloheximide 

Relevant articles and documents

Synthesis and antimicrobial activity of chiral cis-cycloheximide isomers

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Diastereo- and enantioselective synthesis of dimethylcyclohexanamines by asymmetric reductive amination

A series of optically active dimethylcyclohexanamines 6a-c, e, with ee values ranging from 86- > 99%, have been synthesised by asymmetric reductive amination of the corresponding racemic diastereomeric cyclohexanones 3a-c, e. Their conformation and configuration are also discussed.

Preparation of Chiral trans-2,4-Dimethyl-1-cyclohexanones, the Key Intermediates in Cycloheximide Synthesis, Using Microbial Resolution

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