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Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]-

Base Information
  • Chemical Name:Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]-
  • CAS No.:149634-41-3
  • Molecular Formula:C9H10FN3S
  • Molecular Weight:211.263
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10388285
  • Mol file:149634-41-3.mol
Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]-

Synonyms:149634-41-3;Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]-;SCHEMBL940551;DTXSID10388285;AKOS017263432

Suppliers and Price of Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]-
Chemical Property:
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:211.05794667
  • Heavy Atom Count:14
  • Complexity:242
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=NNC(=S)N)C1=CC=CC=C1F
Technology Process of Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]-

There total 2 articles about Hydrazinecarbothioamide, 2-[1-(2-fluorophenyl)ethylidene]- 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:
Guidance literature:
With sodium acetate; In ethanol; for 0.75h; Heating;
Guidance literature:
In benzene; byproducts: isopropanol; moisture excluded; equimolar amt. of ligand added to B compd. in benzene; refluxed for 10-12 h; byproduct fractionated azeotropically with benzene; solvent distd. off; dried in vac.; washed with cyclohexane; dried for 3-4 h; elem. anal.;
DOI:10.1080/00945710009351804
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