4089-03-6

Basic information

• Product Name: (1R,6S)-4β,7,7-Trimethylbicyclo[4.1.0]heptan-3α-ol
• Synonyms: Bicyclo[4.1.0]heptan-3-ol, 4,7,7-trimethyl-, (1R,3S,4S,6S)-
• CAS NO: 4089-03-6
• Molecular Formula: C₁₀H₁₈O
• Molecular Weight: 154.24932
• Mol File: 4089-03-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1R,6S)-4β,7,7-Trimethylbicyclo[4.1.0]heptan-3α-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,6S)-4β,7,7-Trimethylbicyclo[4.1.0]heptan-3α-ol(4089-03-6)
• EPA Substance Registry System: (1R,6S)-4β,7,7-Trimethylbicyclo[4.1.0]heptan-3α-ol(4089-03-6)

Safety Data

• Hazardous Substances Data: 4089-03-6(Hazardous Substances Data)

Upstream product

• 13466-78-9 3-carene 
• 64-17-5 ethanol 
• 4176-01-6 (-)-isocaranone 
• 60-29-7 diethyl ether 
• 936-92-5 (1S,3R,4S,6R)-3,4-epoxy-3,7,7-trimethylbicyclo[4.1.0]heptane 
• 54831-63-9 (-)-cis-caran-trans-4-amine 
• 5208-43-5 (1R,3R,4R,6S)-4,7,7-trimethylbicyclo[4.1.0]hept-3-yl 4-methylbenzenesulfonate 
• 555-31-7 aluminum isopropoxide 
• 67-63-0 isopropyl alcohol 
• 88390-12-9 (-)-cis-car-2-en-4-ol 

Downstream Products

• 5208-43-5 toluene-4-sulfonic acid-((1S,3R,4S)-caran-4-yl ester) 
• 499-70-7 methyl-2 isopropyl-5 cyclohexanone 
• 4176-01-6 cis-carane-4-one 
• 499-70-7 methyl-2 isopropyl-5 cyclohexanone 
• 95242-32-3 2,5,5-trimethylcycloheptanone 
• 4176-02-7 (-)-cis-Caran-3-on-semicarbazon 
• 5208-49-1 cis-4-carene 
• 6909-21-3 (-)-cis-Caran-trans-(5)-ol 
• 4017-88-3 4-isocaranol 
• 4176-01-6 (-)-isocaranone 
• 4175-97-7 4-nitro-benzoic acid-((1S,3R,4S)-caran-4-yl ester) 
• 6617-28-3 phthalic acid mono-((1S,3R,4S)-caran-4-yl ester) 
• 4175-95-5 (-)-4-Caranon-semicarbazon 
• 4176-04-9 (1R,4S,6S)-4,7,7-Trimethyl-bicyclo[4.1.0]heptan-3-one 

Relevant articles and documents

Synthesis of Some 4-Cyanocaranes

Four optically active 4-cyanocaranes diastereoisomers have been synthesized starting from (+)-car-3-ene and their structures supported by chemical evidences and X-ray analysis.

Novel Method for Hydroboration of Olefins Using Electrolysis

A first example of electrochemical hydroboration of olefins was found.Anodic oxidation of sodium borohydride in the presence of olefins in diglyme followed by conventional oxidation gave the corresponding alcohols regio- and stereoselectively in good yields.