Ethyl 6-(acetyloxy)cyclohex-1-ene-1-carboxylate

Base Information Edit

Chemical Name:Ethyl 6-(acetyloxy)cyclohex-1-ene-1-carboxylate
CAS No.:115401-39-3
Molecular Formula:C11H16O4
Molecular Weight:212.246
Hs Code.:
DSSTox Substance ID:DTXSID90552740
Nikkaji Number:J1.942.937G
Mol file:115401-39-3.mol

Synonyms:115401-39-3;Ethyl 6-(acetyloxy)cyclohex-1-ene-1-carboxylate;SCHEMBL8746914;MGDVNYVXDFPUPZ-UHFFFAOYSA-;DTXSID90552740;InChI=1/C11H16O4/c1-3-14-11(13)9-6-4-5-7-10(9)15-8(2)12/h6,10H,3-5,7H2,1-2H3

Suppliers and Price of Ethyl 6-(acetyloxy)cyclohex-1-ene-1-carboxylate

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

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Chemical Property of Ethyl 6-(acetyloxy)cyclohex-1-ene-1-carboxylate Edit

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:212.10485899
Heavy Atom Count:15
Complexity:280

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=CCCCC1OC(=O)C

Technology Process of Ethyl 6-(acetyloxy)cyclohex-1-ene-1-carboxylate

There total 2 articles about Ethyl 6-(acetyloxy)cyclohex-1-ene-1-carboxylate 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: 80.0%

: 28469-52-5
6-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester

: 108-24-7
acetic anhydride

: 115401-39-3
6-acetoxycyclohex-1-enecarboxylic acid ethyl ester

Guidance literature:: With pyridine; at 0 ℃;
DOI:10.1016/S0040-4020(01)81522-2

Reference yield:

: 111-30-8,29257-65-6,79215-57-9
Glutaraldehyde

: 115401-39-3
6-acetoxycyclohex-1-enecarboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; sodium chloride / water / 20 °C

2: dmap; pyridine / 1 h / 20 °C

With pyridine; dmap; potassium carbonate; sodium chloride; In water;