| Identification | Back Directory | [Name]
ISOBORNYL FORMATE | [CAS]
1200-67-5 | [Synonyms]
FEMA 2162
exo-1,7,7-
ISOBORNYL FORMATE
exo-1,7,7-trimethylbicyclo(2.2.1)hept-2
exo-1,7,7-trimethylbicyclo(2.2.1)hept-2r
exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-yl
1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl formate
exo-1,7,7-trimethylbicyclo(2.2.1)hept-2-ylformate
exo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-ylformiat
exo-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ylformiate
1,7,7-trimethyl-,formate,exo-bicyclo[2.2.1]heptan-2-o
formic acid [(2S)-1,7,7-trimethylnorbornan-2-yl] ester
[(6S)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] formate
[(3S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] formate
[(6S)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] methanoate
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, formate, exo-
rel-(1R,2R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl formate
Bicyclo2.2.1heptan-2-ol, 1,7,7-trimethyl-, formate, (1R,2R,4R)-rel-
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, 2-formate, (1R,2R,4R)-rel-
rel-Formic acid (1S*,2S*,4S*)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-yl ester | [EINECS(EC#)]
214-853-3 | [Molecular Formula]
C11H18O2 | [MDL Number]
MFCD00135983 | [MOL File]
1200-67-5.mol | [Molecular Weight]
182.26 |
| Hazard Information | Back Directory | [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.
| [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ChEBI: Isobornyl formate is a bornane monoterpenoid that is isoborneol in which the hydroxy hydrogen has been replaced by a formyl group.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. | [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 |
| Questions And Answer | Back Directory | [Aroma]
ISOBORNYL FORMATE has green-earthy, herbaceous-camphoraceous
odor, more piney than that of the Bornyl
formate, and more camphor-like, less nutlike.
Suggested for use in fruit flavors, and although this ester does have a sweet taste
similar to that of Bornyl formate, it is overall
less fruity or attractive.
The use in fruit flavors amounts to a few
ppm in the finished product (traces). |
|
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BOC Sciences
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https://www.bocsci.com |
| Company Name: |
Energy Chemical
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| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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