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(E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride

Base Information Edit
  • Chemical Name:(E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride
  • CAS No.:100098-81-5
  • Molecular Formula:C15H19 N O3 . Cl H
  • Molecular Weight:297.7772
  • Hs Code.:
  • Mol file:100098-81-5.mol
(E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride

Synonyms:(E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride;(E)-4,5-Dihydro-2-(2-(3,4-dimethoxyphenyl)ethenyl)-4,4-dimethyloxazole hydrochloride;Oxazole, 4,5-dihydro-2-(2-(3,4-dimethoxyphenyl)ethenyl)-4,4-dimethyl-, hydrochloride, (E)-;100098-81-5;LS-100135

Suppliers and Price of (E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride
Supply Marketing:Edit
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 0 raw suppliers
Chemical Property of (E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride Edit
Chemical Property:
  • Vapor Pressure:8.63E-05mmHg at 25°C 
  • Boiling Point:350.9°C at 760 mmHg 
  • Flash Point:135.1°C 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:297.1131712
  • Heavy Atom Count:20
  • Complexity:362
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1(COC(=N1)C=CC2=CC(=C(C=C2)OC)OC)C.Cl
  • Isomeric SMILES:CC1(COC(=N1)/C=C/C2=CC(=C(C=C2)OC)OC)C.Cl
Technology Process of (E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride

There total 3 articles about (E)-2-(3,4-Dimethoxystyryl)-4,4-dimethyl-2-oxazoline hydrochloride 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:
Guidance literature:
With thionyl chloride; In toluene; Ambient temperature;
Guidance literature:
Multi-step reaction with 3 steps
1: SOCl2 / benzene / 0.5 h / 45 - 50 °C
2: CH2Cl2 / 3 h / 0 °C
3: 52.6 percent / SOCl2 / toluene / Ambient temperature
With thionyl chloride; In dichloromethane; toluene; benzene;
Guidance literature:
Multi-step reaction with 2 steps
1: CH2Cl2 / 3 h / 0 °C
2: 52.6 percent / SOCl2 / toluene / Ambient temperature
With thionyl chloride; In dichloromethane; toluene;
Refernces Edit
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