(-)-beta-Fenchyl alcohol

Base Information

• Chemical Name: (-)-beta-Fenchyl alcohol
• CAS No.: 470-08-6
• Molecular Formula: C10H18 O
• Molecular Weight: 154.252
• UNII: 850Y57G047
• DSSTox Substance ID: DTXSID6041183
• Nikkaji Number: J156.723C
• Wikidata: Q27269571
• Mol file: 470-08-6.mol

Synonyms:(-)-beta-Fenchyl alcohol;470-08-6;(-)-beta-Fenchol;(-)-.beta.-Fenchol;beta-Fenchol, (-)-;beta-Fenchyl alcohol, (-)-;(1S,2R,4R)-1,3,3-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-OL;UNII-850Y57G047;(-)-(1S,2R,4R)-beta-Fenchol;850Y57G047;1,3,3-Trimethyl-2-norbornanol, (1S-exo)-;alpha-Fenchol;2-Norbornanol, 1,3,3-trimethyl-, (1S,2R,4R)-(-)-;Bicyclo(2.2.1)heptan-2-ol, 1,3,3-trimethyl-, (1S-exo)-;Bicyclo(2.2.1)heptan-2-ol, 1,3,3-trimethyl-, (1S,2R,4R)-;(1S,2R,4R)-1,3,3-TRIMETHYLBICYCLO(2.2.1)HEPTAN-2-OL;Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1S,2R,4R)-;(1S,2R,4R)-1,3,3-TRIMETHYL-BICYCLO[2.2.1]HEPTAN-2-OL;SCHEMBL9643767;DTXSID6041183;(-)-.BETA.-FENCHYL ALCOHOL;AKOS026742968;.BETA.-FENCHYL ALCOHOL, (-)-;(-)-(1S,2R,4R)-.BETA.-FENCHOL;EN300-181765;Q27269571

Chemical Property of (-)-beta-Fenchyl alcohol

Chemical Property:

• Vapor Pressure: 0.0693mmHg at 25°C
• Boiling Point: 202.9°Cat760mmHg
• PKA: 15.38±0.60(Predicted)
• Flash Point: 73.9°C
• PSA: 20.23000
• Density: 0.992g/cm³
• LogP: 2.19350
• 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%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C2CCC(C2)(C1O)C)C
• Isomeric SMILES: C[C@]12CC[C@H](C1)C([C@@H]2O)(C)C

Technology Process of (-)-beta-Fenchyl alcohol

There total 39 articles about (-)-beta-Fenchyl alcohol 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:

fenchone

fenchyl salicylate

1,3,3-trimethyl-2-norbornanone

(2-Nitro-phenylsulfanylamino)-phenyl-acetic acid (1R,2S,4S)-1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl ester

Refernces

• 1、 Hu, Yi-Ming,Huang, Xiao-Rui,Meng, Zhong-Lei,Qin, Rong-Xiu,Wen, Ru-Si,Zhou, Yong-Hong. "Synthesis of Terpineol from Alpha-Pinene Catalyzed by α-Hydroxy Acids". . . Retrieved 2022/02/17.
• 2、 Yuasa,Nagakura,Tsuruta. "Synthesis and sweetness characteristics of L-aspartyl-D-alanine fenchyl esters". . p. 5013 - 5018. Retrieved 2007/10/03.