Oxazole, 4,5-dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]-

Base Information

Chemical Name:Oxazole, 4,5-dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]-
CAS No.:89393-44-2
Molecular Formula:C15H21NO
Molecular Weight:231.338
Hs Code.:
DSSTox Substance ID:DTXSID10433800
Nikkaji Number:J495.438F

Synonyms:89393-44-2;Oxazole, 4,5-dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]-;DTXSID10433800;4,5-Dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]oxazole

Suppliers and Price of Oxazole, 4,5-dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]-

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

Total 2 raw suppliers

Chemical Property of Oxazole, 4,5-dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]-

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:231.162314293
Heavy Atom Count:17
Complexity:295

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(C)C1=CC=CC=C1C2=NC(CO2)(C)C

Technology Process of Oxazole, 4,5-dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]-

There total 5 articles about Oxazole, 4,5-dihydro-4,4-dimethyl-2-[2-(1-methylpropyl)phenyl]- 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:

: 618-46-2
m-Chlorobenzoyl chloride

: 89393-44-2
2-(2-sec-Butyl-phenyl)-4,4-dimethyl-4,5-dihydro-oxazole

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂ / 14 h / Ambient temperature

2: 70 percent / thionyl chloride / benzene; CH₂Cl₂ / 1.) reflux, 2.) room temperature, 2.5 h

3: 2.) ethanol / 1.) pentane, -78 deg C, 2.) pentane, room temperature

With thionyl chloride; ethanol; In dichloromethane; benzene;
DOI:10.1021/ja00229a037

Reference yield:

: 701923-86-6
3-Chloro-N-(2-hydroxy-1,1-dimethyl-ethyl)-benzamide

: 89393-44-2
2-(2-sec-Butyl-phenyl)-4,4-dimethyl-4,5-dihydro-oxazole

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / thionyl chloride / benzene; CH₂Cl₂ / 1.) reflux, 2.) room temperature, 2.5 h

2: 2.) ethanol / 1.) pentane, -78 deg C, 2.) pentane, room temperature

With thionyl chloride; ethanol; In dichloromethane; benzene;
DOI:10.1021/ja00229a037

Reference yield:

: 535-80-8
3-chlorobenzoate

: 89393-44-2
2-(2-sec-Butyl-phenyl)-4,4-dimethyl-4,5-dihydro-oxazole

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / 1 h / 100 °C

2: CH₂Cl₂ / 14 h / Ambient temperature

3: 70 percent / thionyl chloride / benzene; CH₂Cl₂ / 1.) reflux, 2.) room temperature, 2.5 h

4: 2.) ethanol / 1.) pentane, -78 deg C, 2.) pentane, room temperature

With thionyl chloride; ethanol; In dichloromethane; benzene;
DOI:10.1021/ja00229a037