5-Methyl-1-nonanol

Base Information

Chemical Name:5-Methyl-1-nonanol
CAS No.:2768-16-3
Molecular Formula:C10H22O
Molecular Weight:158.284
Hs Code.:
DSSTox Substance ID:DTXSID00950339
Nikkaji Number:J1.553.127D
Mol file:2768-16-3.mol

Synonyms:5-methylnonan-1-ol;5-METHYL-1-NONANOL;2768-16-3;1-Nonanol, 5-methyl-;SCHEMBL978907;DTXSID00950339;BS-49140;E75071

Suppliers and Price of 5-Methyl-1-nonanol

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 6 raw suppliers

Chemical Property of 5-Methyl-1-nonanol

Chemical Property:

Vapor Pressure:0.0365mmHg at 25°C
Boiling Point:213.4°Cat760mmHg
PKA:15.19±0.10(Predicted)
Flash Point:87.1°C
PSA：20.23000
Density:0.826g/cm³
LogP:2.97530
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:158.167065321
Heavy Atom Count:11
Complexity:71.3

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC(C)CCCCO
Uses 5-Methyl-1-nonanol is a synthesis intermediate. It is used in the preparation of primary alcohols from branched olefins.

Technology Process of 5-Methyl-1-nonanol

There total 1 articles about 5-Methyl-1-nonanol 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:

: 15869-85-9
5-methylnonane

: 2768-15-2
2-butylhexan-1-ol

: 33933-78-7
5-Methyl-5-nonanol

: 2768-16-3
5-methyl-1-nonanol

Guidance literature:: at 90 ℃; beim Behandeln des Reaktionsprodukts mit Lithiumalanat in Aether;

Reference yield:

: 2768-16-3
5-methyl-1-nonanol

: 136539-91-8
(5-Methyl-nonyl)-triphenyl-phosphonium; bromide

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / CBr₄, PPh₃ / CH₂Cl₂ / 0 °C

2: 100 percent / acetonitrile / 48 h / Heating

With carbon tetrabromide; triphenylphosphine; In dichloromethane; acetonitrile;