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(Z)-3-Fluoro-2-phenylallylamine

Base Information
  • Chemical Name:(Z)-3-Fluoro-2-phenylallylamine
  • CAS No.:93605-75-5
  • Molecular Formula:C9H10FN
  • Molecular Weight:151.184
  • Hs Code.:
  • Mol file:93605-75-5.mol
(Z)-3-Fluoro-2-phenylallylamine

Synonyms:(Z)-3-Fluoro-2-phenyl-2-propen-1-amine;(Z)-3-Fluoro-2-phenylallylamine

Suppliers and Price of (Z)-3-Fluoro-2-phenylallylamine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (Z)-3-Fluoro-2-phenylallylamine
Chemical Property:
  • PSA:26.02000 
  • LogP:2.65600 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of (Z)-3-Fluoro-2-phenylallylamine

There total 9 articles about (Z)-3-Fluoro-2-phenylallylamine 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 hydrazine hydrate; In methanol; for 3h; Heating;
DOI:10.1016/j.bmc.2005.09.065
Guidance literature:
Multi-step reaction with 8 steps
1.1: lithium diisopropylamide / tetrahydrofuran / 0.5 h / -78 °C
1.2: 87 percent / tetrahydrofuran / 3 h / -78 - 20 °C
2.1: NaH / tetrahydrofuran / 0 °C
2.2: tetrahydrofuran / 120 h / 20 °C
3.1: 110 °C
4.1: 65 percent / diisobutylaluminum hydride / tetrahydrofuran; hexane / 3 h / -78 - 5 °C
5.1: 82 percent / Ph3P; diethyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C
6.1: bromine / CH2Cl2 / 24 h
7.1: 38 percent / NaI / acetone / 4 h / Heating
8.1: hydrazine hydrate / methanol / 3 h / Heating
With bromine; sodium hydride; diisobutylaluminium hydride; hydrazine hydrate; triphenylphosphine; sodium iodide; lithium diisopropyl amide; diethylazodicarboxylate; In tetrahydrofuran; methanol; hexane; dichloromethane; acetone; 5.1: Mitsunobu reaction;
DOI:10.1016/j.bmc.2005.09.065
Guidance literature:
Multi-step reaction with 4 steps
1: 82 percent / Ph3P; diethyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C
2: bromine / CH2Cl2 / 24 h
3: 38 percent / NaI / acetone / 4 h / Heating
4: hydrazine hydrate / methanol / 3 h / Heating
With bromine; hydrazine hydrate; triphenylphosphine; sodium iodide; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; acetone; 1: Mitsunobu reaction;
DOI:10.1016/j.bmc.2005.09.065
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