Tert-butyl 4-oxoimidazolidine-1-carboxylate

Base Information

Chemical Name:Tert-butyl 4-oxoimidazolidine-1-carboxylate
CAS No.:885954-76-7
Molecular Formula:C₈H₁₄N₂O₃
Molecular Weight:186.211
Hs Code.:
DSSTox Substance ID:DTXSID20402729
Wikidata:Q82206200
Mol file:885954-76-7.mol

Synonyms:Tert-butyl 4-oxoimidazolidine-1-carboxylate;885954-76-7;1-Boc-4-oxoimidazolidine;1-Imidazolidinecarboxylic acid, 4-oxo-, 1,1-dimeth;SCHEMBL14686817;DTXSID20402729;VHHMYPLTJYOOMG-UHFFFAOYSA-N;MFCD04038548;AKOS006294388;DS-4915;Tert-butyl4-oxoimidazolidine-1-carboxylate;F84484;EN300-7411777;A861717;4-oxoimidazolidine-1-carboxylic acid tert-butyl ester

Suppliers and Price of Tert-butyl 4-oxoimidazolidine-1-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
Packaging
price

Crysdot
tert-Butyl4-oxoimidazolidine-1-carboxylate 95%
1g
$ 78.00

Crysdot
tert-Butyl4-oxoimidazolidine-1-carboxylate 95%
10g
$ 392.00

Crysdot
tert-Butyl4-oxoimidazolidine-1-carboxylate 95%
5g
$ 236.00

Chemenu
tert-butyl4-oxoimidazolidine-1-carboxylate 95%
1g
$ 442.00

Alichem
tert-Butyl4-oxoimidazolidine-1-carboxylate
10g
$ 399.00

Alichem
tert-Butyl4-oxoimidazolidine-1-carboxylate
5g
$ 234.84

Total 17 raw suppliers

Chemical Property of Tert-butyl 4-oxoimidazolidine-1-carboxylate

Chemical Property:

XLogP3:0.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:186.10044231
Heavy Atom Count:13
Complexity:232

Purity/Quality:

97% ^*data from raw suppliers

tert-Butyl4-oxoimidazolidine-1-carboxylate 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)N1CC(=O)NC1

Technology Process of Tert-butyl 4-oxoimidazolidine-1-carboxylate

There total 1 articles about Tert-butyl 4-oxoimidazolidine-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: 96.0%

: 1253964-00-9
tert-butyl 4-oxo-2-thioxoimidazolidine-1-carboxylate

: 885954-76-7
tert-butyl 4-oxoimidazolidine-1-carboxylate

Guidance literature:: tert-butyl 4-oxo-2-thioxoimidazolidine-1-carboxylate; With nickel dichloride; In methanol; Inert atmosphere;

With sodium tetrahydroborate; In methanol; at 0 - 23 ℃; for 1h; Inert atmosphere;

With acetic acid; In methanol; Inert atmosphere;
DOI:10.1021/acs.orglett.1c02134

Reference yield:

: 885954-76-7
tert-butyl 4-oxoimidazolidine-1-carboxylate

: 91047-77-7
ethyl (2E)-3-(2-bromophenyl)prop-2-enoate

: tert-butyl (E)-3-(2-(3-(hydroxyamino)-3-oxoprop-1-en-1-yl)phenyl)-4-oxoimidazolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium phosphate; (R,R)-N,N'-dimethyl-1,2-diaminocyclohexane; copper(l) iodide / N,N-dimethyl-formamide / 3 h / 100 °C / Microwave irradiation

2: hydroxylamine; sodium hydroxide / water; tetrahydrofuran; methanol / 18 h / 20 °C

With potassium phosphate; copper(l) iodide; (R,R)-N,N'-dimethyl-1,2-diaminocyclohexane; hydroxylamine; sodium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;