100400-22-4

Basic information

• Product Name: 1-hydroxy-2-isopropyl-5-methyl-cyclohexanecarbonitrile
• Synonyms: 1-hydroxy-2-isopropyl-5-methyl-cyclohexanecarbonitrile
• CAS NO: 100400-22-4
• Molecular Weight: 181.278
• Mol File: 100400-22-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-hydroxy-2-isopropyl-5-methyl-cyclohexanecarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 1-hydroxy-2-isopropyl-5-methyl-cyclohexanecarbonitrile(100400-22-4)
• EPA Substance Registry System: 1-hydroxy-2-isopropyl-5-methyl-cyclohexanecarbonitrile(100400-22-4)

Safety Data

• Hazardous Substances Data: 100400-22-4(Hazardous Substances Data)

Upstream product

• 74-90-8 hydrogen cyanide 
• 10458-14-7 (2R,5S)-menthone 
• 7677-24-9 trimethylsilyl cyanide 

Downstream Products

• 143-33-9 sodium cyanide 
• 10458-14-7 Menthone 
• 1040504-85-5 (1R,2S,5R)-1-cyano-2-isopropyl-5-methylcyclohexyl (R)-2-methoxy-2-phenylacetate 
• 1040504-91-3 (1R,2S,5R)-1-cyano-2-isopropyl-5-methylcyclohexyl (S)-2-methoxy-2-phenylacetate 
• 367939-60-4 (1R,2S,5R)-1-aminomethyl-2-iso-propyl-5-methylcyclohexan-1-ol 
• 74-90-8 hydrogen cyanide 
• 10458-14-7 (2R,5S)-menthone 

Relevant articles and documents

New chiral iodooxazoline catalysts for the I(III)-mediated α-tosyloxylation of ketones: Refining the stereoinduction model

A new family of iodooxazoline catalysts, derived from widely available chiral ketones (menthone and camphor), was developed to promote the iodine(III)-mediated α-tosyloxylation of ketone derivatives. The reaction conditions to achieve the direct formation

Absolute configuration of ketone cyanohydrins by 1H nmr: The special case of polar substituted tertiary alcohols

The absolute configuration of ketone cyanohydrins can be assigned from analysis of the 1H NMR spectra of the corresponding (R)-and (S)-MPA ester derivatives and use of ΔδRS signs. This is an application of the NMR methodology for ste