CAS 76-49-3

(±)-Bornylacetat

Formel: C₁₂H₂₀O₂

InChl: 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

InChI Key: InChIKey=KGEKLUUHTZCSIP-QJUVKGSQNA-N

SMILES: C[C@@]12[C@H](OC(C)=O)C[C@@](C1(C)C)(CC2)[H]

Synonyme:

• 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

Bornyl Acetate

CAS: 76-49-3

Bornyl Acetate

Formel: C₁₂H₂₀O₂

Reinheit: >97%,mixtures

Molekulargewicht: 196.29

Ref: 54-OR1030105

Bornyl acetate

CAS: 76-49-3

Bornyl acetate

Formel: C₁₂H₂₀O₂

Reinheit: 99%

Molekulargewicht: 196.29

Ref: 54-BUP14902

Bornyl acetate

CAS: 76-49-3

Bornyl acetate (Isobornyl acetate) has an anti-inflammatory effect. It is the volatile ingredient in some Chinese traditional herbs and numerous conifer oils.

Formel: C₁₂H₂₀O₂

Reinheit: 98% - 99.19%

Farbe und Form: Liquid

Molekulargewicht: 196.286

Ref: TM-T1246

Bornyl acetate (Standard)

CAS: 76-49-3

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.

Formel: C₁₂H₂₀O₂

Farbe und Form: Solid

Molekulargewicht: 196.286

Ref: TM-TMSM-3000

Bornyl Acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Farbe und Form: Colorless Liquid

Molekulargewicht: 196.29

Ref: 4Z-B-145001

rel-(1R,2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Reinheit: 97%

Farbe und Form: Liquid

Molekulargewicht: 196.2860

Ref: IN-DA0038GL

Bornyl acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Reinheit: 95%~99%

Molekulargewicht: 196.29

Ref: BP-BP0280

Bornyl Acetate (Mixture of Diastereomers)

CAS: 76-49-3

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)

Formel: C₁₂H₂₀O₂

Farbe und Form: Neat

Molekulargewicht: 196.29

Ref: TR-B675555

Bornyl acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Reinheit: ≥ 90.0%

Farbe und Form: Clear, colourless to pale yellow liquid

Molekulargewicht: 196.29

Ref: 7W-GY0324

Bornyl Acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Molekulargewicht: 196.29

Ref: ST-EA-CP-CS58130

Bornyl acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Farbe und Form: Colourless solid; Sweet herbaceous odour

Molekulargewicht: 196.29

Ref: BE-RMCB174000

Bornyl acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Farbe und Form: Colourless solid; Sweet herbaceous odour

Molekulargewicht: 196.29

Ref: BE-RMT21190-20ml

Bornyl acetate

CAS: 76-49-3

Formel: C₁₂H₂₀O₂

Farbe und Form: Colourless solid; Sweet herbaceous odour

Molekulargewicht: 196.29

Ref: BE-RMT21190

Bornyl acetate

CAS: 76-49-3

rel-(1R,2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate

Formel: C₁₂H₂₀O₂

Reinheit: 98%

Molekulargewicht: 196.29

Ref: IN-DG118582

(+/-)-Bornyl acetate

CAS: 76-49-3

(-)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>br

Formel: C₁₂H₂₀O₂

Reinheit: Min. 95%

Farbe und Form: Clear Liquid

Molekulargewicht: 196.29 g/mol

Ref: 3D-FB74112