Ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate

Base Information

Chemical Name:Ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate
CAS No.:80912-42-1
Molecular Formula:C₁₆H₂₀FN₃O₃
Molecular Weight:321.352
Hs Code.:
European Community (EC) Number:279-624-2
DSSTox Substance ID:DTXSID501001636
Nikkaji Number:J320.346H
Wikidata:Q82995621
Mol file:80912-42-1.mol

Synonyms:80912-42-1;ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate;EINECS 279-624-2;Ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro(4.5)decane-8-carboxylate;SCHEMBL11043785;MPLUISYIZALWBE-UHFFFAOYSA-N;DTXSID501001636;NS00060635;Ethyl 1-(4-fluorophenyl)-4-hydroxy-1,3,8-triazaspiro[4.5]dec-3-ene-8-carboxylate;ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4,5]decane-8-carboxylate

Suppliers and Price of Ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate

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
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Total 6 raw suppliers

Chemical Property of Ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate

Chemical Property:

Vapor Pressure:6.25E-12mmHg at 25°C
Boiling Point:544.9°C at 760 mmHg
Flash Point:283.3°C
PSA：65.37000
Density:1.32g/cm³
LogP:1.98930
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:321.14886967
Heavy Atom Count:23
Complexity:458

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)N1CCC2(CC1)C(=O)NCN2C3=CC=C(C=C3)F

Technology Process of Ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate

There total 1 articles about Ethyl 1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decane-8-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: