468-68-8

  • Product Name:drimenol
  • Molecular Formula:C15H26 O
  • Molecular Weight:222.371
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Product Details

pd_meltingpoint:98 °C

Purity:99%

High Quality Chinese Factory supply 468-68-8 drimenol

  • Molecular Formula:C15H26 O
  • Molecular Weight:222.371
  • Vapor Pressure:0.000125mmHg at 25°C 
  • Melting Point:98 °C 
  • Boiling Point:298.8°Cat760mmHg 
  • PKA:14.82±0.10(Predicted) 
  • Flash Point:106.9°C 
  • PSA:20.23000 
  • Density:0.921g/cm3 
  • LogP:3.77750 

(-)-Drimenol(Cas 468-68-8) Usage

Definition

ChEBI: A sesquiterpenoid primary alcohol, being methanol in which one of the methyl hydrogens is substituted by a 2,5,5,8a-tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl group.

InChI:InChI=1/C15H26O/c1-11-6-7-13-14(2,3)8-5-9-15(13,4)12(11)10-16/h6,12-13,16H,5,7-10H2,1-4H3/t12-,13-,15+/m0/s1

468-68-8 Relevant articles

Practical isolation of polygodial from Tasmannia lanceolata: A viable scaffold for synthesis

Just, Jeremy,Jordan, Timothy B.,Paull, Brett,Bissember, Alex C.,Smith, Jason A.

, p. 11200 - 11207 (2015)

Polygodial, a valuable sesquiterpene dia...

TERPENOIC ACID GLYCERIDES FROM THE DORID NUDIBRANCH ARCHIDORIS MONTEREYENSIS

Gustafson, Kirk,Andersen, Raymond J.,Chen, Marie H.M.,Clardy, Jon,Hochlowski, Jill E.

, p. 11 - 14 (1984)

Extracts of the dorid nudibranch Archido...

Elimination of C-8-functional groups from driman-8α,11-diol-11- monoacetate and-diacetate

Kuchkova,Aryku,Barba,Vlad

, p. 412 - 416 (2007)

The dehydration products of driman-8α,11...

Synthesis of 11-aminodrim-7-ene from drimenol

Kuchkova,Arycu,Vlad

, p. 367 - 370 (2009)

11-Aminodrim-7-ene was synthesized from ...

Synthesis and bio-inspired optimization of drimenal: Discovery of chiral drimane fused oxazinones as promising antifungal and antibacterial candidates

Li, Dangdang,Zhang, Shasha,Song, Zehua,Li, Wei,Zhu, Feng,Zhang, Jiwen,Li, Shengkun

supporting information, p. 558 - 567 (2017/12/07)

The synthesis of antifungal natural prod...

Enzymatic Addition of Alcohols to Terpenes by Squalene Hopene Cyclase Variants

Kühnel, Lisa C.,Nestl, Bettina M.,Hauer, Bernhard

, p. 2222 - 2225 (2017/10/09)

Squalene–hopene cyclases (SHCs) catalyze...

Synthesis and structure-activity relationships for cytotoxicity and apoptosis-inducing activity of (+)-halichonine B

Hayakawa, Ichiro,Nakamura, Tomomi,Ohno, Osamu,Suenaga, Kiyotake,Kigoshi, Hideo

, p. 9969 - 9976 (2015/10/12)

Halichonine B is a sesquiterpene alkaloi...

468-68-8 Process route

Farnesol
106-28-5

Farnesol

(+/-)-drim-7-en-11-ol
468-68-8,19078-37-6,54750-55-9,84108-05-4,84108-08-7,90457-95-7,90457-96-8

(+/-)-drim-7-en-11-ol

Conditions
Conditions Yield
With fluorosulphonic acid; In various solvent(s); at -75 ℃;
71%
With fluorosulphonic acid; In various solvent(s); at -85 - -80 ℃; for 0.116667h;
57.9%
With fluorosulphonic acid; In dichloromethane; at -78 ℃; for 1h;
52%
With fluorosulphonic acid; 1-butyl-3-methylimidazolium Tetrafluoroborate; In dichloromethane; at -45 ℃; for 0.25h;
36%
With mercuric triflate; N,N-dimethyl-aniline; Multistep reaction; 1.) -20 deg C, 2 h, nitromethane;
With fluorosulphonic acid; In dichloromethane; at -115 - -110 ℃; Yield given;
(2E,6E)-3,7,11-trimethyldodeca-2,6,11-trien-1-ol
161835-52-5

(2E,6E)-3,7,11-trimethyldodeca-2,6,11-trien-1-ol

(+/-)-drim-7-en-11-ol
468-68-8,19078-37-6,54750-55-9,84108-05-4,84108-08-7,90457-95-7,90457-96-8

(+/-)-drim-7-en-11-ol

Conditions
Conditions Yield
With fluorosulphonic acid; In various solvent(s); at -80 ℃; for 0.666667h;
77.9%

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