Fenchol

Base Information

• Chemical Name: Fenchol
• CAS No.: 1632-73-1
• Deprecated CAS: 10378-33-3,2217-01-8,2217-01-8
• Molecular Formula: C₁₀H₁₈O
• Molecular Weight: 154.252
• European Community (EC) Number: 216-639-5,208-135-9
• DSSTox Substance ID: DTXSID1041970
• Nikkaji Number: J7.537J
• Wikipedia: Fenchol
• Wikidata: Q417941
• Metabolomics Workbench ID: 125298
• ChEMBL ID: CHEMBL1907996
• Mol file: 1632-73-1.mol

Synonyms:2-Norbornanol,1,3,3-trimethyl- (6CI,7CI,8CI);1,3,3-Trimethyl-2-norbornanol;1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol;2-Fenchanol;Fenchyl alcohol;

Chemical Property of Fenchol

Chemical Property:

• Appearance/Colour: colorless to pale yellow solid or liquid
• Vapor Pressure: 0.069mmHg at 25°C
• Melting Point: 43-46 °C
• Refractive Index: 1.502
• Boiling Point: 202.9 °C at 760 mmHg
• PKA: 15.38±0.60(Predicted)
• Flash Point: 73.9 °C
• PSA: 20.23000
• Density: 0.992 g/cm³
• LogP: 2.19350
• Storage Temp.: 2-8°C
• Solubility.: Chloroform, Ethanol (Sparingly), Methanol (Slightly)
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 154.135765193
• Heavy Atom Count: 11
• Complexity: 185

Purity/Quality:

99.9% ^*data from raw suppliers

Fenchyl Alcohol >96.0%(GC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 22-24/25-26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C2CCC(C2)(C1O)C)C
• Description: Fenchyl alcohol has a camphor-like odor with citrus notes and a bitter, lime-like flavor. It is synthesized by reduction of fenchone or from pine terpenes.
• Uses: Fenchol is a hop-derived aroma compound commonly found in beer.

Technology Process of Fenchol

There total 28 articles about Fenchol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

fenchone (4695-62-9,126-21-6) → Fenchol (4695-62-9,470-08-6,512-13-0,1632-73-1,2217-02-9,14575-74-7,22627-95-8,36386-49-9,36386-50-2,64439-31-2)

Guidance literature:

With ethanol; sodium; dl-fenchyl alcohol;

Reference yield:

→ Fenchol (4695-62-9,470-08-6,512-13-0,1632-73-1,2217-02-9,14575-74-7,22627-95-8,36386-49-9,36386-50-2,64439-31-2)

Guidance literature:

With ethanol; sodium; Ld"-fenchyl alcohol;

Reference yield:

ethanedioic acid 1,2-bis(1,3,3-trimethylbicyclo[2.2.1]hept-2-yl)ester (124118-33-8) → Fenchol (4695-62-9,470-08-6,512-13-0,1632-73-1,2217-02-9,14575-74-7,22627-95-8,36386-49-9,36386-50-2,64439-31-2)

Guidance literature:

With potassium hydroxide; inactive fenchyl alcohol;

upstream raw materials:

1,3,3-trimethyl-2-norbornanone

fenchone

ethanedioic acid 1,2-bis(1,3,3-trimethylbicyclo[2.2.1]hept-2-yl)ester

(+)-α-pinene

Downstream raw materials:

fenchyl salicylate

1,3,3-trimethyl-2-norbornanone

cyclofenchene

fenchone

Refernces

• 1、 Grabovskiy,Khalitova,Fedorova,Lobov,Rol’nik,Kabal’nova. "Synthesis and kinetic regularities of the thermal decomposition of new hydrotrioxides of cyclic alcohols". . p. 464 - 468. Retrieved 2017/03/08.
• 2、 Janusz,Gardklik,Young,Burkes,Stoll,Estelle,Riley. "High potency dipeptide sweeteners. 1. L-aspartyl-D-phenylglycine esters". . p. 1052 - 1061. Retrieved 2007/10/02.