Ebanol

Base Information

Chemical Name:Ebanol
CAS No.:67801-20-1
Molecular Formula:C14H24O
Molecular Weight:208.344
Hs Code.:
European Community (EC) Number:267-140-4
Nikkaji Number:J317.147G
RXCUI:2383933
Mol file:67801-20-1.mol

Synonyms:3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol;ebanol

Suppliers and Price of Ebanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Chem-Impex
3-Methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol,90-100%(GC),KOSHER,FEMA4775Hazmat 90-100%(GC)
25G
$ 29.12

American Custom Chemicals Corporation
EBANOL 95.00%
5MG
$ 497.51

AHH
Ebanol 90%
1000ml
$ 445.00

Total 29 raw suppliers

Chemical Property of Ebanol

Chemical Property:

Vapor Pressure:0.000281mmHg at 25°C
Refractive Index:1.522
Boiling Point:287.3 °C at 760 mmHg
PKA:14.96±0.20(Predicted)
Flash Point:103.5 °C
PSA：20.23000
Density:0.938 g/cm³
LogP:4.61090
Water Solubility.:34mg/L at 20℃
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:208.182715385
Heavy Atom Count:15
Complexity:273

Purity/Quality:

99.9% ^*data from raw suppliers

3-Methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol,90-100%(GC),KOSHER,FEMA4775Hazmat 90-100%(GC) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CCC(C1(C)C)C=CC(C)C(C)O
Isomeric SMILES:CC1=CCC(C1(C)C)/C=C/C(C)C(C)O

Technology Process of Ebanol

There total 5 articles about Ebanol 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: 94.5%

: (1'S)-(E)-3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-one

: sodium borohydrid

: 96-22-0
pentan-3-one

: 67801-20-1
3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol

(E)-3-Methyl-5-(2,2,3-trimethylcylcopent-3-en-1-yl)pent-4-en-2-ol: (E)-3-Methyl-5-(2,2,3-trimethylcylcopent-3-en-1-yl)pent-4-en-2-ol

Guidance literature:: With sodium hydroxide; In ethanol; water;

Reference yield:

: 67801-15-4
3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-one

: 67801-20-1
3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol

Guidance literature:: With aluminum tri-sec-butoxide; iso-butanol; at 115 ℃; for 5h; Reagent/catalyst; Temperature;

Reference yield:

: 4501-58-0,23727-15-3,91200-86-1,91819-58-8
campholenyc aldehyde

: 67801-20-1
3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / water / 6 h / -10 - 40 °C

2.1: sodium hydroxide / water; cyclohexane / 3 h / 40 °C

2.2: 7 h / 70 - 75 °C

3.1: aluminum tri-sec-butoxide; iso-butanol / 5 h / 115 °C

With aluminum tri-sec-butoxide; iso-butanol; potassium hydroxide; sodium hydroxide; In cyclohexane; water;