Ethyl 3-bromo-1-ethyl-2-oxocyclohexane-1-carboxylate

Base Information

Chemical Name:Ethyl 3-bromo-1-ethyl-2-oxocyclohexane-1-carboxylate
CAS No.:89816-94-4
Molecular Formula:C11H17BrO3
Molecular Weight:277.15500
Hs Code.:
DSSTox Substance ID:DTXSID70523796

Synonyms:89816-94-4;Ethyl 3-bromo-1-ethyl-2-oxocyclohexanecarboxylate;Ethyl 3-bromo-1-ethyl-2-oxocyclohexane-1-carboxylate;starbld0019579;DTXSID70523796

Suppliers and Price of Ethyl 3-bromo-1-ethyl-2-oxocyclohexane-1-carboxylate

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 Ethyl 3-bromo-1-ethyl-2-oxocyclohexane-1-carboxylate

Chemical Property:

PSA：43.37000
LogP:2.46240
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:276.03611
Heavy Atom Count:15
Complexity:265

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1(CCCC(C1=O)Br)C(=O)OCC

Technology Process of Ethyl 3-bromo-1-ethyl-2-oxocyclohexane-1-carboxylate

There total 2 articles about Ethyl 3-bromo-1-ethyl-2-oxocyclohexane-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: 90.0%

: 55443-01-1
ethyl 2-oxo-1-ethyl-1-cyclohexanecarboxylate

: 89816-94-4
ethyl 3-bromo-1-ethyl-2-oxocyclohexanecarboxylate

Guidance literature:: With bromine; In water; for 4h; Ambient temperature;

Reference yield:

: 1655-07-8
ethyl 2-oxocyclohexane carboxylate

: 89816-94-4
ethyl 3-bromo-1-ethyl-2-oxocyclohexanecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / sodium hydride / tetrahydrofuran / Ambient temperature; overnight

2: 90 percent / bromine / H₂O / 4 h / Ambient temperature

With bromine; sodium hydride; In tetrahydrofuran; water;