4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-

Base Information

Chemical Name:4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-
CAS No.:58461-27-1
Deprecated CAS:1845-51-8
Molecular Formula:C10H18 O
Molecular Weight:154.252
Hs Code.:
European Community (EC) Number:261-264-2
UNII:1YPC7F65XU
DSSTox Substance ID:DTXSID70866690
Nikkaji Number:J296.944K
Wikipedia:Lavandulol
Wikidata:Q616128
Mol file:58461-27-1.mol

Synonyms:2-isopropenyl-5-methyl-4-hexen-1-ol;4-hexen-1-ol, 5-methyl-2-(1-methylethenyl)-;5-methyl-2-(1-methylethenyl)-4-hexen-1-ol;lavandulol

Suppliers and Price of 4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-

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

TRC
rac-Lavandulol
100mg
$ 1010.00

TRC
rac-Lavandulol
10mg
$ 125.00

Sigma-Aldrich
Lavandulol analytical standard
50mg
$ 366.00

J&W Pharmlab
(+/-)-Lavandulol 95%
250mg
$ 175.00

J&W Pharmlab
(+/-)-Lavandulol 95%
100mg
$ 137.00

J&W Pharmlab
(+/-)-Lavandulol 95%
500mg
$ 249.00

J&W Pharmlab
(+/-)-Lavandulol 95%
5g
$ 1398.00

J&W Pharmlab
(+/-)-Lavandulol 95%
1g
$ 398.00

Crysdot
5-Methyl-2-(prop-1-en-2-yl)hex-4-en-1-ol 95+%
5g
$ 831.00

Chemenu
5-Methyl-2-(prop-1-en-2-yl)hex-4-en-1-ol 95%
5g
$ 777.00

Total 29 raw suppliers

Chemical Property of 4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-

Chemical Property:

Vapor Pressure:0.0127mmHg at 25°C
Refractive Index:n20/D 1.470
Boiling Point:230.2°Cat760mmHg
PKA:14.81±0.10(Predicted)
Flash Point:88.3°C
PSA：20.23000
Density:0.857g/cm³
LogP:2.52730
Storage Temp.:2-8°C
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:154.135765193
Heavy Atom Count:11
Complexity:152

Purity/Quality:

97% ^*data from raw suppliers

rac-Lavandulol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 23-24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCC(CO)C(=C)C)C
Uses A fragrance of lavender oil. The fragrance of the nature-identical (R)-enantiomer ('weak floral, herbal odor with slightly lemon-like, fresh citrus fruity nuance') was superior to those of both the unnatural (S)-enantiomer ('very weak odor') and the racemate ('weak floral, herbal odor'). A fragrance of lavender oil. The fragrance of the nature-identical (R)-enantiomer (''weak floral, herbal odor with slightly lemon-like, fresh citrus fruity nuance'') was superior to those of both the unnatural (S)-enantiomer (''very weak odor'') and the racemate (''weak floral, herbal odor'').

Technology Process of 4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-

There total 71 articles about 4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)- 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: 97.0%

: 25905-14-0,50373-59-6
lavandulyl acetate

: 58461-27-1,21090-68-6
(+/-)-lavandulol

Guidance literature:: With potassium hydroxide; In ethanol; for 3h; Ambient temperature;

Reference yield: 95.0%

: 1845-54-1
(±)-ethyl 5-methyl-2-(prop-1-en-2-yl)hex-4-enoate

: 58461-27-1,21090-68-6
(+/-)-lavandulol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20 ℃; for 1.33333h; Inert atmosphere;
DOI:10.1021/jo500027k