Oxazole, 2-(2-ethenyl-3-methoxyphenyl)-4,5-dihydro-4,4-dimethyl-

Base Information

Chemical Name:Oxazole, 2-(2-ethenyl-3-methoxyphenyl)-4,5-dihydro-4,4-dimethyl-
CAS No.:143123-58-4
Molecular Formula:C14H17NO2
Molecular Weight:231.294
Hs Code.:
DSSTox Substance ID:DTXSID40448109
Nikkaji Number:J495.424F
Wikidata:Q82267052

Synonyms:143123-58-4;Oxazole, 2-(2-ethenyl-3-methoxyphenyl)-4,5-dihydro-4,4-dimethyl-;DTXSID40448109;4,5-Dihydro-4,4-dimethyl-2-(2-ethenyl-3-methoxyphenyl)oxazole

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Oxazole, 2-(2-ethenyl-3-methoxyphenyl)-4,5-dihydro-4,4-dimethyl-

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:231.125928785
Heavy Atom Count:17
Complexity:322

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(COC(=N1)C2=C(C(=CC=C2)OC)C=C)C

Technology Process of Oxazole, 2-(2-ethenyl-3-methoxyphenyl)-4,5-dihydro-4,4-dimethyl-

There total 5 articles about Oxazole, 2-(2-ethenyl-3-methoxyphenyl)-4,5-dihydro-4,4-dimethyl- 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: 91.0%

: 57598-32-0
4,5-dihydro-2-(2',3'-dimethoxyphenyl)-4,4-dimethyloxazole

: 1826-67-1
vinyl magnesium bromide

: 143123-58-4
2-(3-Methoxy-2-vinylphenyl)-4,4-dimethyl-2-oxazoline

Guidance literature:: In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jo000750r

Reference yield:

: 57598-32-0
4,5-dihydro-2-(2',3'-dimethoxyphenyl)-4,4-dimethyloxazole

: 917-57-7
vinyllithium

: 143123-58-4
2-(3-Methoxy-2-vinylphenyl)-4,4-dimethyl-2-oxazoline

Guidance literature:: In tetrahydrofuran; at -45 ℃; for 3h;
DOI:10.1021/jo00401a018

Reference yield:

: 1521-38-6
2,3-dimethoxybenzoic acid

: 143123-58-4
2-(3-Methoxy-2-vinylphenyl)-4,4-dimethyl-2-oxazoline

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂

3: SOCl₂

4: tetrahydrofuran

With thionyl chloride; In tetrahydrofuran; 1: Substitution / 2: Acylation / 3: Cyclization / 4: Substitution;
DOI:10.1016/S0040-4039(99)00907-7