CAS 76-49-3
:(±)-Acétate de bornyle
Formule :C12H20O2
InChI :InChI=1/C12H20O2/c1-8(13)14-10-7-9-5-6-12(10,4)11(9,2)3/h9-10H,5-7H2,1-4H3/t9-,10+,12+/s2
Code InChI :InChIKey=KGEKLUUHTZCSIP-QJUVKGSQNA-N
SMILES :C[C@@]12[C@H](OC(C)=O)C[C@@](C1(C)C)(CC2)[H]
Synonymes :- 1,7,7-Trimethylbicyclo(2.2.1)heptan-2-ol acetate
- 1,7,7-Trimethylbicyclo(2.2.1)heptan-2-yl acetate, endo-
- 2-Camphanol acetate
- 2-Camphanyl acetate
- Acetate de endo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yle
- Acetate, 1,7,7-Trimethyl-Bicyclo(2.2.1)Hept-2-Yl, Endo-
- Acetato De Endo-1,7,7-Trimetilbiciclo[2.2.1]Hept-2-Ilo
- Ai3-00665
- Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, 2-acetate, (1R,2S,4R)-rel-
- Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, acetate, (1R,2S,4R)-rel-
- Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, acetate, endo-
- Borneol, acetate
- Borneol, acetate (8CI)
- Borneyl acetate
- Bornyl acetic ester
- Bornyl acetic ether
- Bornyl ethanoate
- Endo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl aceatate
- FEMA No. 2159
- Nsc 407158
- dl-Bornyl acetate
- endo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-yl acetate
- endo-1,7,7-Trimethylbicyclo[2.2.1]hept-2-ylacetat
- endo-2-Camphanyl ethanoate
- endo-Bornyl acetate
- Voir plus de synonymes
Filtrer par
Pourcentage de pureté
0
100
|
0
|
50
|
90
|
95
|
100
15 produits trouvés.
- Tri par prix ascendant
- Tri par prix descendant
- Puretés inférieures
- Puretés supérieures
- Livraison estimée la plus rapide
Bornyl Acetate
CAS :Bornyl AcetateFormule :C12H20O2Degré de pureté :>97%,mixturesMasse moléculaire :196.29Bornyl acetate
CAS :Bornyl acetate (Isobornyl acetate) has an anti-inflammatory effect. It is the volatile ingredient in some Chinese traditional herbs and numerous conifer oils.Formule :C12H20O2Degré de pureté :98% - 99.19%Couleur et forme :LiquidMasse moléculaire :196.286Bornyl acetate (Standard)
CAS :Bornyl acetate (Standard) is a reference standard for research and analysis in studies involving Bornyl acetate. Bornyl acetate (Isobornyl acetate) has an anti-inflammatory effect. It is the volatile ingredient in some Chinese traditional herbs and numerous conifer oils.Formule :C12H20O2Couleur et forme :SolidMasse moléculaire :196.286rel-(1R,2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate
CAS :Formule :C12H20O2Degré de pureté :97%Couleur et forme :LiquidMasse moléculaire :196.2860Bornyl Acetate (Mixture of Diastereomers)
CAS :Applications Bornyl Acetate (Mixture of Diastereomers) is a monoterpene ester, and also the main, natural constituent of valerian root oil. Bornyl acetate also has analgesic and anti-inflammatory properties.
References Buchbauer, G., et al.: Die Pharm., 47, 620 (1992); Oh, H., et al.: Appl. Micro., 15, 777 (1967); Wu, X., et al.: J. Chinese Med. Mat., 27, 438 (2004)Formule :C12H20O2Couleur et forme :NeatMasse moléculaire :196.29Bornyl acetate
CAS :Formule :C12H20O2Degré de pureté :≥ 90.0%Couleur et forme :Clear, colourless to pale yellow liquidMasse moléculaire :196.29Bornyl acetate
CAS :Formule :C12H20O2Couleur et forme :Colourless solid; Sweet herbaceous odourMasse moléculaire :196.29Bornyl acetate
CAS :Formule :C12H20O2Couleur et forme :Colourless solid; Sweet herbaceous odourMasse moléculaire :196.29Bornyl acetate
CAS :Formule :C12H20O2Couleur et forme :Colourless solid; Sweet herbaceous odourMasse moléculaire :196.29Bornyl acetate
CAS :rel-(1R,2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetateFormule :C12H20O2Degré de pureté :98%Masse moléculaire :196.29(+/-)-Bornyl acetate
CAS :(-)Bornyl acetate is a natural product that has been shown to have antimicrobial properties. It is extracted from plants such as the Boronia and has been shown to inhibit the growth of bacteria. (-)Bornyl acetate interacts with hydroxyl groups on proteins, inhibiting their function. This interaction leads to the production of reactive oxygen species, which causes cellular damage and death. Bornyl acetate also can interact with other sites on proteins, including the nitro group, which may lead to reduced nitric oxide production and decreased inflammatory response. The compound class of (-)bornyl acetate includes alkanoic acids and fatty acids. Molecular docking analysis has identified a number of possible binding sites for this molecule in protein structures. -Bornyl acetate is not active against viruses or fungi.br>br> Bornyl acetate has been shown to be an anti-inflammatory agent that inhibits prostaglandin synthesis and exhibits anti-infective properties.br>brFormule :C12H20O2Degré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :196.29 g/mol










