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3-Methoxy-4-aminostilbene

Base Information Edit
  • Chemical Name:3-Methoxy-4-aminostilbene
  • CAS No.:73928-02-6
  • Molecular Formula:C15H15NO
  • Molecular Weight:225.29
  • Hs Code.:
  • Nikkaji Number:J61.339H
  • Mol file:73928-02-6.mol
3-Methoxy-4-aminostilbene

Synonyms:3-Methoxy-4-aminostilbene;3-Methoxy-4-stilbenamine;73928-02-6;4-Stilbenamine, 3-methoxy-;BRN 3132628;2-methoxy-4-[(E)-2-phenylethenyl]aniline;4-13-00-02242 (Beilstein Handbook Reference);Benzenamine, 2-methoxy-4-(2-phenylethenyl)-;LS-146777

Suppliers and Price of 3-Methoxy-4-aminostilbene
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
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 3-METHOXY-4-STILBENAMINE 95.00%
  • 5MG
  • $ 503.44
Total 3 raw suppliers
Chemical Property of 3-Methoxy-4-aminostilbene Edit
Chemical Property:
  • Vapor Pressure:2.58E-06mmHg at 25°C 
  • Refractive Index:1.5200 (estimate) 
  • Boiling Point:390.8°C at 760 mmHg 
  • Flash Point:197.7°C 
  • PSA:35.25000 
  • Density:1.132g/cm3 
  • LogP:4.02900 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:225.115364102
  • Heavy Atom Count:17
  • Complexity:245
Purity/Quality:

99% *data from raw suppliers

3-METHOXY-4-STILBENAMINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=CC(=C1)C=CC2=CC=CC=C2)N
  • Isomeric SMILES:COC1=C(C=CC(=C1)/C=C/C2=CC=CC=C2)N
Technology Process of 3-Methoxy-4-aminostilbene

There total 4 articles about 3-Methoxy-4-aminostilbene 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:
Multi-step reaction with 2 steps
2: aq.-ethanolic HCl
With hydrogenchloride;
Guidance literature:
Multi-step reaction with 2 steps
2: aq.-ethanolic HCl
With hydrogenchloride;
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