ISOBORNYL FORMATE
ISOBORNYL FORMATE Basic information
- Product Name:
- ISOBORNYL FORMATE
- Synonyms:
-
- ISOBORNYL FORMATE
- FEMA 2162
- 1,7,7-trimethyl-,formate,exo-bicyclo[2.2.1]heptan-2-o
- 1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl formate
- Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, formate, exo-
- exo-1,7,7-
- [(3S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] formate
- exo-1,7,7-trimethylbicyclo(2.2.1)hept-2
- CAS:
- 1200-67-5
- MF:
- C11H18O2
- MW:
- 182.26
- EINECS:
- 214-853-3
- Mol File:
- 1200-67-5.mol
ISOBORNYL FORMATE Chemical Properties
- Boiling point:
- 213.6±7.0 °C(Predicted)
- Density
- 1.02±0.1 g/cm3(Predicted)
- FEMA
- 2162 | ISOBORNYL FORMATE
- storage temp.
- Sealed in dry,Room Temperature
- Odor
- at 100.00 %. camphor musty medical woody
- Odor Type
- balsamic
- JECFA Number
- 1390
- LogP
- 3.19
- EPA Substance Registry System
- Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, formate, (1R,2R,4R)-rel- (1200-67-5)
ISOBORNYL FORMATE Usage And Synthesis
Description
Isobornyl formate has a characteristic aromatic, pine needles odor. May be prepared by reaction of formic acid with camphene in the presence of a catalyst; also in the absence of a catalyst; the resulting products do not exhibit well-defined optical characteristics. The corresponding optically active esters have been prepared from d- or ι-camphene and formic acid in the presence of phthalic anhydride.
Chemical Properties
Isobornyl formate has a characteristic aromatic, pine needles odor.
Preparation
By reaction of formic acid with camphene in the presence of a catalyst; also in the absence of a catalyst; the resulting products do not exhibit well-defined optical characteristics. The corresponding optically active esters have been prepared from d- or l-camphene and formic acid in the presence of phthalic anhydride
Definition
ChEBI: Isobornyl formate is a bornane monoterpenoid that is isoborneol in which the hydroxy hydrogen has been replaced by a formyl group. It has a role as a plant metabolite. It is a bornane monoterpenoid, a bridged compound and a formate ester. It is functionally related to a borneol.
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