N-Phenyl-4-methyloxazolidine-2-imine

Base Information

Chemical Name:N-Phenyl-4-methyloxazolidine-2-imine
CAS No.:25240-99-7
Molecular Formula:C₁₀H₁₂N₂O
Molecular Weight:176.218
Hs Code.:
DSSTox Substance ID:DTXSID501260501
Nikkaji Number:J1.141.609H

Synonyms:DTXSID501260501;N-Phenyl-4-methyloxazolidine-2-imine;4,5-Dihydro-4-methyl-N-phenyl-2-oxazolamine;25240-99-7

Suppliers and Price of N-Phenyl-4-methyloxazolidine-2-imine

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 N-Phenyl-4-methyloxazolidine-2-imine

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:176.094963011
Heavy Atom Count:13
Complexity:197

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1COC(=N1)NC2=CC=CC=C2

Technology Process of N-Phenyl-4-methyloxazolidine-2-imine

There total 6 articles about N-Phenyl-4-methyloxazolidine-2-imine 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: 77.0%

: 21152-53-4
1-(1-hydroxypropan-2-yl)-3-phenylthiourea

: 25240-99-7
4,5-dihydro-4-methyl-N-phenyl-2-oxazolamine

Guidance literature:: With sodium hydroxide; p-toluenesulfonyl chloride; In tetrahydrofuran; water; at 20 ℃; for 0.5h;
DOI:10.1016/S0040-4020(01)00682-2

Reference yield: 32.0%

: 223600-50-8
1-(2-hydroxy-1-methyl-ethyl)-3-phenyl-urea

: 25240-99-7
4,5-dihydro-4-methyl-N-phenyl-2-oxazolamine

: 33609-38-0
4-methyl-1-phenyl-2-imidazolidinone

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 0.583333h;
DOI:10.1080/00397919908086441

Reference yield:

: 103-71-9
phenyl isocyanate

: 25240-99-7
4,5-dihydro-4-methyl-N-phenyl-2-oxazolamine

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 20 °C

2: 32 percent / triphenylphosphine; diethyl azodicarboxylate / tetrahydrofuran / 0.58 h / 20 °C

With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1: Addition / 2: Mitsunobu reaction;
DOI:10.1080/00397919908086441