ChemicalBook > Product Catalog > Organic Chemistry > Alcohols,Phenols,Phenol alcohols > thuj-4(10)-en-3-ol
thuj-4(10)-en-3-ol
thuj-4(10)-en-3-ol Basic information
- Product Name:
- thuj-4(10)-en-3-ol
- Synonyms:
-
- thuj-4(10)-en-3-ol
- sabinol
- (1S,5S)-1-Isopropyl-4-methylenebicyclo[3.1.0]hexan-3-ol
- (1S,3R,5S)-1-isopropyl-4-methylene-bicyclo[3.1.0]hexan-3-ol
- (1S,3R,5S)-4-methylidene-1-propan-2-yl-bicyclo[3.1.0]hexan-3-ol
- (1S,3R,5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexan-3-ol
- (+)-cis-sabinol
- CAS:
- 471-16-9
- MF:
- C10H16O
- MW:
- 152.23
- EINECS:
- 207-436-2
- Mol File:
- 471-16-9.mol
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thuj-4(10)-en-3-ol Chemical Properties
- Boiling point:
- 208°C (estimate)
- Density
- 0.9488
- refractive index
- 1.4871 (estimate)
- pka
- 14.85±0.40(Predicted)
- LogP
- 2.215 (est)
- EPA Substance Registry System
- Bicyclo[3.1.0]hexan-3-ol, 4-methylene-1-(1-methylethyl)-, (1S,3R,5S)- (471-16-9)
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thuj-4(10)-en-3-ol Usage And Synthesis
Definition
ChEBI: (+)-cis-sabinol is a sabinol. It is an enantiomer of a (-)-cis-sabinol.
Synthesis
Sabinol is produced: 1) Many patented syntheses start from Citronellol. One method uses autoxidation, followed by reduction and finally, acid-catalyzed cyclization. 2) from Crotonaldehyde and Vinylether via Ethoxymethyl dihydropyran. Hydration, followed by a reaction with iso-butenyl magnesium bromide, leads to Rose oxide.