(R)-2-Methyl-1-octanol

Base Information

Chemical Name:(R)-2-Methyl-1-octanol
CAS No.:120925-50-0
Molecular Formula:C9H20O
Molecular Weight:144.257
Hs Code.:
UNII:33G823889O
Nikkaji Number:J715.982J
Wikidata:Q27256266
Mol file:120925-50-0.mol

Synonyms:(R)-2-Methyl-1-octanol;2-Methyloctanol, (R)-;(-)-2-Methyl-1-octanol;(2R)-2-Methyl-1-octanol;1-Octanol, 2-methyl-, (R)-;1-Octanol, 2-methyl-, (2R)-;UNII-33G823889O;33G823889O;120925-50-0;(R)-2-methyloctanol;SCHEMBL8417136;Q27256266

Suppliers and Price of (R)-2-Methyl-1-octanol

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 1 raw suppliers

Chemical Property of (R)-2-Methyl-1-octanol

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:6
Exact Mass:144.151415257
Heavy Atom Count:10
Complexity:61.7

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(C)CO
Isomeric SMILES:CCCCCC[C@@H](C)CO

Technology Process of (R)-2-Methyl-1-octanol

There total 2 articles about (R)-2-Methyl-1-octanol 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:

: 1159491-82-3
4-({[(2R)-2-methyloctyl]oxy}carbonyl)benzoic acid

: 100-21-0
terephthalic acid

: 120925-50-0
(R)-2-methyloctan-1-ol

Guidance literature:: With sodium hydroxide; In methanol; dichloromethane;

Reference yield:

: 72748-99-3,187035-29-6
(R)-1-Amino-2-(methoxymethyl)pyrrolidine

: 120925-50-0
(R)-2-methyloctan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 16 h / 20 °C

2.1: lithium tetramethylpiperidide / tetrahydrofuran / 1 h / 0 °C

2.2: tetrahydrofuran / 16 h / -100 °C

3.1: 4 mol/l HCl / pentane / 0.25 h / 20 °C

4.1: BH₃*SMe₂ / diethyl ether / 0.75 h / 20 °C

With hydrogenchloride; dimethylsulfide borane complex; 2,2,6,6-tetramethylpiperidinyl-lithium; In tetrahydrofuran; diethyl ether; pentane;
DOI:10.1016/S0040-4039(02)00595-6