(R)-2-Isopropyl-5-methylhexanol

Base Information

Chemical Name:(R)-2-Isopropyl-5-methylhexanol
CAS No.:41884-28-0
Molecular Formula:C10H22 O
Molecular Weight:158.284
Hs Code.:2905199090
European Community (EC) Number:255-573-1
DSSTox Substance ID:DTXSID80885852
Nikkaji Number:J59.033I
Wikidata:Q82864548
Mol file:41884-28-0.mol

Synonyms:(R)-2-Isopropyl-5-methylhexanol;41884-28-0;1-Hexanol, 5-methyl-2-(1-methylethyl)-, (2R)-;(2R)-5-methyl-2-propan-2-ylhexan-1-ol;EINECS 255-573-1;DTXSID80885852;(R)-2-isopropyl-5-methylhexan-1-ol;[R,(+)]-2-Isopropyl-5-methyl-1-hexanol;(2R)-5-methyl-2-(propan-2-yl)hexan-1-ol;1-Hexanol, 5-methyl-2-(1-methylethyl)-, (R)-

Suppliers and Price of (R)-2-Isopropyl-5-methylhexanol

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

Total 4 raw suppliers

Chemical Property of (R)-2-Isopropyl-5-methylhexanol

Chemical Property:

Vapor Pressure:0.0423mmHg at 25°C
Boiling Point:211°Cat760mmHg
PKA:15.00±0.10(Predicted)
Flash Point:79.9°C
PSA：20.23000
Density:0.823g/cm³
LogP:2.68710
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:158.167065321
Heavy Atom Count:11
Complexity:86.9

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CCC(CO)C(C)C
Isomeric SMILES:CC(C)CC[C@@H](CO)C(C)C

Technology Process of (R)-2-Isopropyl-5-methylhexanol

There total 7 articles about (R)-2-Isopropyl-5-methylhexanol 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: 87.0%

: 87017-28-5
(R)-2-Isopropyl-5-methyl-hexanoic acid ethyl ester

: 41884-28-0
(R)-(+)-Tetrahydrolavandulol

Guidance literature:: With lithium aluminium tetrahydride;
DOI:10.1016/S0040-4039(01)90020-6

Reference yield:

: 498-16-8,21090-68-6
(R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-ol

: 41884-28-0
(R)-(+)-Tetrahydrolavandulol

Guidance literature:: With platinum(IV) oxide; acetic acid ester; Hydrogenation_.zuletzt in Eisessig;

Reference yield:

: 97-41-6,1802-02-4,7377-84-6,15543-65-4,16642-27-6,34909-55-2,41641-25-2,41641-26-3,41641-27-4
ethyl chrysanthemate

: 41884-28-0
(R)-(+)-Tetrahydrolavandulol

Guidance literature:: Multi-step reaction with 3 steps

1: 47 percent / methanesulfonic acid / 1,2-dichloro-ethane / 2 h / 70 °C

2: 86 percent / H₂ / PtO₂

3: 87 percent / LiAlH₄

With lithium aluminium tetrahydride; methanesulfonic acid; hydrogen; platinum(IV) oxide; In 1,2-dichloro-ethane;
DOI:10.1016/S0040-4039(01)90020-6