CAS 2217-02-9
:(+)-Fenchol
- (+)-Fenchol
- (+)-Fenchol~1,3,3-Trimethyl-2-norbornanol
- (+)-Fenchyl alcohol
- (+)-α-Fenchol
- (+)-α-Fenchyl alcohol
- (1R)-endo-(+)-Fenchyl alcohol
- (1R,2R,4S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
- (1R,2S,4S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
- (2R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
- 1,3,3-Trimethyl-2-norbornanol
- <span class="text-smallcaps">D</span>-Fenchol
- <span class="text-smallcaps">D</span>-Fenchyl alcohol
- Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1R,2R,4S)-
- See more synonyms
(1R)-endo-(+)-Fenchyl alcohol, 96%
CAS:(1R)-endo-(+)-Fenchyl alcohol can be extensively used in daily chemicals such as fair antiperspirant, textile softener and liquid detergent. It can also be esterified by different kinds of organic acids to expand its usage in flavors and fragrances. This Thermo Scientific Chemicals brand product was
Formula:C10H18OPurity:96%Color and Shape:Colorless to white to pale cream, Crystals or powder or crystalline powder or fused solid or clear liquid as meltMolecular weight:154.25(+)-Fenchol
CAS:(+)-Fenchol analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C10H18OPurity:(GC) ≥98%Color and Shape:LiquidMolecular weight:154.25(+)-Fenchol
CAS:(+)-Fenchol, a monoterpenoid discovered in various plants including Cannabis, serves both as a precursor in synthesizing other terpenoids and as a chiral building block for the organic synthesis of numerous compounds. Additionally, formulations incorporating (+)-fenchol are employed as fragrance ingredients.Formula:C10H18OColor and Shape:SolidMolecular weight:154.3(+)-Fenchyl alcohol 100 µg/mL in Methanol
CAS:Formula:C10H18OColor and Shape:Single SolutionMolecular weight:154.25Smart Solutions™ TerpiMix Kit 2500 μg/mL in Isopropanol
CAS:Controlled Product- 10458-14-7
- 105-87-3
- 106-22-9
- 106-24-1
- 106-25-2
- 111-02-4
- 112-14-1
- 1139-30-6
- 116-26-7
- 1196-01-6
- 123-35-3
- 124-76-5
- 125-12-2
- 127-91-3
- 13466-78-9
- 138-86-3
- 13877-91-3
- 2217-02-9
- 2244-16-8
- 22567-21-1
- 3387-41-5
- 4602-84-0
- 4630-07-3
- 464-43-7
- 464-45-9
- 4674-50-4
- 469-61-4
- 4695-62-9
- 470-82-6
- 489-86-1
- 498-15-7
- 499-75-2
- 502-61-4
- 515-69-5
- 527-84-4
- 535-77-3
- 5392-40-5
- 546-79-2
- 546-80-5
- 562-74-3
- 586-62-9
- 638-36-8
- 675-20-7
- 6753-98-6
- 7212-44-4
- 7541-49-3
- 76-22-2
- 77-53-2
- 7787-20-4
- 78-70-6
- 79-92-5
- 80-56-8
- 87-44-5
- 89-78-1
- 89-79-2
- 89-81-6
- 89-82-7
- 89-83-8
- 98-55-5
- 99-83-2
- 99-85-4
- 99-86-5
- 99-87-6
Color and Shape:Kit(1R)-Endo-(+)-fenchyl alcohol
CAS:(1R)-Endo-(+)-fenchyl alcohol is a chemotype of terpenes. Terpenes are hydrocarbons that are the major constituent of many essential oils and resins. The most well-known terpene is limonene, which is found in the rinds of citrus fruits. Terpenes are important for their flavors and aromas. They also have a variety of industrial uses, such as in fragrances and flavorings, paints, varnishes, and coatings. This particular chemotype has an equilibration time of 1-2 minutes at room temperature and can be prepared by evaporation or headspace techniques. (1R)-Endo-(+)-fenchyl alcohol has been detected in the aroma of grapefruit peel oil with a sensitivity of 0.5 ng/l air sample. It can be quantified using gas chromatography with flame ionization detection at 0.1 μg/l air sample or
Formula:C10H18OPurity:Min. 97%Color and Shape:White PowderMolecular weight:154.25 g/mol










