1-Cyclohexyl-2-tricyclo[3.3.1.13,7]dec-1-ylethanone

Base Information

Chemical Name:1-Cyclohexyl-2-tricyclo[3.3.1.13,7]dec-1-ylethanone
CAS No.:76308-70-8
Molecular Formula:C₁₈H₂₈O
Molecular Weight:260.42
Hs Code.:
DSSTox Substance ID:DTXSID401224718

Synonyms:1-Cyclohexyl-2-tricyclo[3.3.1.13,7]dec-1-ylethanone;DTXSID401224718;AKOS000345896;AKOS000423114;76308-70-8

Suppliers and Price of 1-Cyclohexyl-2-tricyclo[3.3.1.13,7]dec-1-ylethanone

Supply Marketing:

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

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Chemical Property of 1-Cyclohexyl-2-tricyclo[3.3.1.13,7]dec-1-ylethanone

Chemical Property:

XLogP3:5.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:260.214015512
Heavy Atom Count:19
Complexity:323

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)C(=O)CC23CC4CC(C2)CC(C4)C3

Technology Process of 1-Cyclohexyl-2-tricyclo[3.3.1.13,7]dec-1-ylethanone

There total 2 articles about 1-Cyclohexyl-2-tricyclo[3.3.1.13,7]dec-1-ylethanone 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: 92.0%

: 19835-38-2
1-adamantylacetyl chloride

: 53398-24-6
Adamantan-1-yl-acetic acid cyclohexyl ester

: 76308-70-8
1-cyclohexyl-2-(1-adamantyl)-1-ethanone

Guidance literature:: With cuprous halogenide; In diethyl ether; for 1h; Heating;

Reference yield:

: 108-85-0
1-bromocyclohexane

: 19835-38-2
1-adamantylacetyl chloride

: 76308-70-8
1-cyclohexyl-2-(1-adamantyl)-1-ethanone

Guidance literature:: With copper(I) chloride; magnesium; Yield given. Multistep reaction; 1.)Et₂O 2.)boiled;

Reference yield:

: 76308-70-8
1-cyclohexyl-2-(1-adamantyl)-1-ethanone

: 76308-59-3
α-cyclohexyl-1-adamantylethylamine hydrochloride

Guidance literature:: With acetamide; hydrogenchloride; formic acid; Yield given. Multistep reaction; 1.) reflux 8.5 h, 2.) reflux, 6 h;
DOI:10.1007/BF00765659