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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: 2026-07-07 18:25:53
  • (-)-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 endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl acetate
L-Bornyl acetate, R
1,7,7-trimethyl-,acetate,(1s-endo)-bicyclo[2.2.1]htan-2-o
(1S,2R,4S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl acetate
Bornyl acetate,endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]ht-2-yl acetate
Bornyl Acetate Standd
(contains ca. Isobornyl Acetate)
(-)-BORNYL ACETATE WITH
Borneyl Acetate
(-)-BORNYL ACETATE
Bornyl ethanoate
(1S,2R,4S)-bornyl acetate
(-)-[(1S)-bornyl]-acetate
Bornyl Acetate (contains ca. Isobornyl Acetate)>
(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]htan-2-yl acetate
endo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-yl acetate
EINECS 243-750-6
(1S,4β)-1α,7,7-Trimethylbicyclo[2.2.1]htan-2α-ol acetate
ENDO-(1R)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HT-2-YL-ACETATE
Bicyclo2.2.1htan-2-ol, 1,7,7-trimethyl-, acetate, (1S,2R,4S)
[1S,2R,4S,(-)]-Borneol acetate
MFCD00135942
BORNYL ACETATE, L
(1S,4S,4β)-1,7,7-Trimethylbicyclo[2.2.1]htan-2α-ol acetate
Levo-bornyl acetate
ENDO-(1S)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HT-2-YL ACETATE
endo-bornyl acetate
L-(-)-BORNYL ACETATE
Bornyl Acetate (contains ca. Isobornyl Acetate)
Borneol, acetate, (1S,2R,4S)-(-)
(-)-Bornyl acetate
(1S,2R,4S)-1,7,7-Trimethyl-bicyclo[2.2.1]ht-2-yl acetate
1,7,7-trimethyl-,acetate,(1S-endo)-Bicyclo[2.2.1]htan-2-ol
L-born-2-yl acetate
L-BORNYL ACETATE
L-BORNYL ACETIC ETHER
BORNYLACETAT FLUESSIG
Bornyl Acetate,contains ca. Isobornyl Acetate
Bornyl Acetate
[(1R,3S)-4,7,7-trimethyl-3-bicyclo[2.2.1]htanyl] acetate
(1S,2R,4S)-1,7,7-Trimethylbicyclo[2.2.1]hept-2-ylacetat
Acetic acid (1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]htane-2-yl ester
Bicyclo[2.2.1]htan-2-ol,1,7,7-trimethyl-,acetate,(1S-endo)
L-Bornyl Acetate (AS)
Borneol Acetate
(-)-Bornyl acetate, 10 mM in DMSO
L-alpha-bornyl acetate
LAEVO-BORNYLACETATE
Bornyl Acetic ester
L-BORNEOL ACETATE
ACETIC ACID L-BORNYL ESTER
(−)-Bornyl acetate
endo-2-Camphanyl ethanoate
endo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acetate
BORNYL ACETATE, L-(SG)
(-)-Borneol acetate
[1S,4S,(-)]-1,7,7-Trimethylbicyclo[2.2.1]htan-2α-ol acetate
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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