1-Undecanol, 3-methyl-, 4-methylbenzenesulfonate, (S)-

Base Information

Chemical Name:1-Undecanol, 3-methyl-, 4-methylbenzenesulfonate, (S)-
CAS No.:131906-80-4
Molecular Formula:C₁₉H₃₂O₃S
Molecular Weight:340.527
Hs Code.:
DSSTox Substance ID:DTXSID501211328

Synonyms:1-Undecanol, 3-methyl-, 4-methylbenzenesulfonate, (S)-;DTXSID501211328;131906-80-4

Suppliers and Price of 1-Undecanol, 3-methyl-, 4-methylbenzenesulfonate, (S)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1-Undecanol, 3-methyl-, 4-methylbenzenesulfonate, (S)-

Chemical Property:

XLogP3:6.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:12
Exact Mass:340.20721605
Heavy Atom Count:23
Complexity:378

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCC(C)CCOS(=O)(=O)C1=CC=C(C=C1)C
Isomeric SMILES:CCCCCCCC[C@H](C)CCOS(=O)(=O)C1=CC=C(C=C1)C

Technology Process of 1-Undecanol, 3-methyl-, 4-methylbenzenesulfonate, (S)-

There total 5 articles about 1-Undecanol, 3-methyl-, 4-methylbenzenesulfonate, (S)- 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: 99.0%

: 121404-69-1
(S)-(-)-3-methylundecan-1-ol

: 98-59-9
p-toluenesulfonyl chloride

: 131906-80-4
(S)-1-(p-toluenesulfonyloxy)-3-methylundecane

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃;
DOI:10.1021/jo0497961

Reference yield:

: 709027-78-1
(S)-3-methyl-1-(tert-butyldimethylsilyloxy)undecane

: 131906-80-4
(S)-1-(p-toluenesulfonyloxy)-3-methylundecane

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / AcCl / methanol / 20 °C

2: 99 percent / pyridine / CH₂Cl₂ / 20 °C

With pyridine; acetyl chloride; In methanol; dichloromethane;
DOI:10.1021/jo0497961

Reference yield:

: 67601-05-2,67650-82-2
(3S)-3,7-dimethyl-6-octen-1-yl acetate

: 131906-80-4
(S)-1-(p-toluenesulfonyloxy)-3-methylundecane

Guidance literature:: Multi-step reaction with 4 steps

1: 1) ozone, 2) dimethyl sulfide / 1) MeOH, -78 deg C, 2) -10 deg C, 1 h, then ice-bath temperature, 1 h, then r.t., 1 h

3: 85 percent / LiAlH₄, CoCl₂ / tetrahydrofuran / 12 h / Ambient temperature

4: 2.4 g / pyridine / 12 h / 0 - 5 °C

With pyridine; lithium aluminium tetrahydride; dimethylsulfide; ozone; In tetrahydrofuran;