1-Ethyl-1-cyclododecanol

Base Information

Chemical Name:1-Ethyl-1-cyclododecanol
CAS No.:16313-36-3
Molecular Formula:C₁₄H₂₈O
Molecular Weight:212.376
Hs Code.:
European Community (EC) Number:653-317-7

Synonyms:1-ETHYL-1-CYCLODODECANOL;SCHEMBL6062608;AKOS024334109

Suppliers and Price of 1-Ethyl-1-cyclododecanol

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

Sigma-Aldrich
1-ETHYL-1-CYCLODODECANOL AldrichCPR
250mg
$ 57.00

Total 1 raw suppliers

Chemical Property of 1-Ethyl-1-cyclododecanol

Chemical Property:

XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:212.214015512
Heavy Atom Count:15
Complexity:141

Purity/Quality:

98%,99%, ^*data from raw suppliers

1-ETHYL-1-CYCLODODECANOL AldrichCPR ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1(CCCCCCCCCCC1)O

Technology Process of 1-Ethyl-1-cyclododecanol

There total 2 articles about 1-Ethyl-1-cyclododecanol 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:

: 925-90-6
ethylmagnesium bromide

: 830-13-7
cyclododecanone

: 16313-36-3
1-Aethyl-cyclododecanol-⁽¹⁾

Guidance literature:: DOI:10.1016/S0040-4020(01)92842-X

Reference yield:

: 16313-36-3
1-Aethyl-cyclododecanol-⁽¹⁾

Guidance literature:: Cyclododecanon, Aethyl-magnesiumbromid;

Reference yield:

: 16313-36-3
1-Aethyl-cyclododecanol-⁽¹⁾

: 1357255-91-4
12-hydroxy-12-phenyltetradecanal

Guidance literature:: Multi-step reaction with 2 steps

1.1: boron trifluoride diethyl etherate / dichloromethane / 1.5 h / 0 °C / Inert atmosphere

1.2: 2.5 h / -78 °C

1.3: -78 - 20 °C

2.1: trimethylsilyl trifluoromethanesulfonate; triphenylphosphine / dichloromethane / 1 h / 20 °C / Inert atmosphere

2.2: 0.17 h / 20 °C / Inert atmosphere

2.3: 2 h / 40 °C

With trimethylsilyl trifluoromethanesulfonate; boron trifluoride diethyl etherate; triphenylphosphine; In dichloromethane;
DOI:10.1002/anie.201106046