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5655-61-8

5655-61-8 structure
5655-61-8 structure
  • Name: Bornyl acetate
  • Chemical Name: l-bornyl acetate
  • CAS Number: 5655-61-8
  • Molecular Formula: C12H20O2
  • Molecular Weight: 196.286
  • Catalog: Chemical reagent Organic reagent Ester Other ester compounds
  • Create Date: 2018-02-09 08:00:00
  • Modify Date: 2024-01-02 18:13:41
  • (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].
Name l-bornyl acetate
Synonyms Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, acetate, (1S,2R,4S)-
(1S,2R,4S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-ylacetat
endo-bornyl acetate
Bornyl ethanoate
endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl acetate
(-)-Bornyl acetate
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, acetate, (1S,2R,4S)-
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, acetate, (1S-endo)-
Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, acetate, endo-
L-born-2-yl acetate
(1S,2R,4S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl acetate
endo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-yl acetate
Borneol Acetate
EINECS 243-750-6
Bornyl Acetic ester
MFCD00135942
(−)-Bornyl acetate
Borneol, acetate, (1S,2R,4S)-(-)-
Borneyl Acetate
endo-2-Camphanyl ethanoate
endo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acetate
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, acetate, endo-
Description (-)-Bornyl acetate (L-(-)-Bornyl acetate), isolated from hyssop oil, is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate possesses antifungal activity[1].
Related Catalog
Target

Human Endogenous Metabolite

In Vitro The wavy roots from seedlings exposed to (-)-bornyl acetate are significantly longer than those from seedlings exposed to ()-bornyl acetate[1]. (-)-Bornyl acetate (L-bornyl acetate), when applied individually to barley seedlings, reduced powdery mildew infection compared with controls not containing ether[2].
References

[1]. Jun-Ichiro Horiuchi, et al. Exposing Arabidopsis seedlings to borneol and bornyl acetate affects root growth: Specificity due to the chemical and optical structures of the compounds. Journal of Plant Interactions Volume 2, 2007 - Issue 2.

[2]. M. P. LETESSIER ETESSIE, et al. Antifungal Activity of the Essential Oil of Hyssop (Hyssopus offcinalis). J. Phytopathology 149, 673±678 (2001).
Density 1.0±0.1 g/cm3
Boiling Point 223.5±0.0 °C at 760 mmHg
Melting Point 29ºC
Molecular Formula C12H20O2
Molecular Weight 196.286
Flash Point 84.4±0.0 °C
Exact Mass 196.146332
PSA 26.30000
LogP 3.60
Vapour Pressure 0.1±0.4 mmHg at 25°C
Index of Refraction 1.480
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xn
Risk Phrases R20/21/22
Safety Phrases S24/25
RIDADR NA 1993 / PGIII
WGK Germany 1

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title: CAS No. 5655-61-8 | Chemsrc address: https://www.chemsrc.com/en/baike/766312.html

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