(2S,4S)-4-Methyl-2-(2-methylpropyl)oxane

Base Information

Chemical Name:(2S,4S)-4-Methyl-2-(2-methylpropyl)oxane
CAS No.:16665-10-4
Molecular Formula:C₁₀H₂₀O
Molecular Weight:156.268
Hs Code.:
DSSTox Substance ID:DTXSID70506827
Wikidata:Q82362770
Mol file:16665-10-4.mol

Synonyms:(2S,4S)-4-Methyl-2-(2-methylpropyl)oxane;16665-10-4;SCHEMBL15678357;DTXSID70506827

Suppliers and Price of (2S,4S)-4-Methyl-2-(2-methylpropyl)oxane

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of (2S,4S)-4-Methyl-2-(2-methylpropyl)oxane

Chemical Property:

Vapor Pressure:1.13mmHg at 25°C
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:156.151415257
Heavy Atom Count:11
Complexity:109

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCOC(C1)CC(C)C
Isomeric SMILES:C[C@H]1CCO[C@H](C1)CC(C)C

Technology Process of (2S,4S)-4-Methyl-2-(2-methylpropyl)oxane

There total 5 articles about (2S,4S)-4-Methyl-2-(2-methylpropyl)oxane 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:

: 488-05-1
3-methyl-1-(3-methylfuran-2-yl)butan-1-one

: 5206-80-4,13477-62-8,16665-10-4,91527-21-8,140237-69-0,140237-70-3,140238-78-4,140238-79-5
cis-2-(2-methylpropyl)-4-methyltetrahydropyran

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / LiAlH₄ / diethyl ether / 6 h / 0 °C

2: 3.0 g / H₂ / W-4 Raney nickel / ethanol / 35 - 40 °C / 54340 Torr

3: 56 percent / active alumina / pyridine / 255 °C

4: H₂ / Adam's catalyst / acetic acid

With aluminum oxide; lithium aluminium tetrahydride; hydrogen; platinum(IV) oxide; W-4 Raney nickel; In pyridine; diethyl ether; ethanol; acetic acid;

Reference yield:

: 16891-23-9
2-isobutyl-4-methyl-5,6-dihydro-4H-pyran

: 5206-80-4,13477-62-8,16665-10-4,91527-21-8,140237-69-0,140237-70-3,140238-78-4,140238-79-5
cis-2-(2-methylpropyl)-4-methyltetrahydropyran

Guidance literature:: With hydrogen; platinum(IV) oxide; In acetic acid; Yield given;

Reference yield:

: 82684-26-2,91603-60-0
3-methyl-1-(3-methyl-2-furyl)-1-butanol

: 5206-80-4,13477-62-8,16665-10-4,91527-21-8,140237-69-0,140237-70-3,140238-78-4,140238-79-5
cis-2-(2-methylpropyl)-4-methyltetrahydropyran

Guidance literature:: Multi-step reaction with 3 steps

1: 3.0 g / H₂ / W-4 Raney nickel / ethanol / 35 - 40 °C / 54340 Torr

2: 56 percent / active alumina / pyridine / 255 °C

3: H₂ / Adam's catalyst / acetic acid

With aluminum oxide; hydrogen; platinum(IV) oxide; W-4 Raney nickel; In pyridine; ethanol; acetic acid;