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5-Fhdpat

Base Information Edit
  • Chemical Name:5-Fhdpat
  • CAS No.:127126-21-0
  • Molecular Formula:C16H24FNO
  • Molecular Weight:265.371
  • Hs Code.:
  • UNII:1G916IMD7L
  • DSSTox Substance ID:DTXSID201034408,DTXSID30925792
  • Nikkaji Number:J322.179B
  • Wikipedia:UH-301
  • Wikidata:Q27088892
  • Pharos Ligand ID:SSHJBQVTSTGX
  • ChEMBL ID:CHEMBL22778
  • Mol file:127126-21-0.mol
5-Fhdpat

Synonyms:5-FHDPAT;5-fluoro-8-hydroxy-2-(dipropylamino)tetralin;UH 301;UH-301

Suppliers and Price of 5-Fhdpat
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
Total 2 raw suppliers
Chemical Property of 5-Fhdpat Edit
Chemical Property:
  • Vapor Pressure:2.22E-06mmHg at 25°C 
  • Boiling Point:382°Cat760mmHg 
  • Flash Point:184.8°C 
  • Density:1.08g/cm3 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:265.18419255
  • Heavy Atom Count:19
  • Complexity:268
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCCN(CCC)C1CCC2=C(C=CC(=C2C1)O)F
  • Isomeric SMILES:CCCN(CCC)[C@H]1CCC2=C(C=CC(=C2C1)O)F
Technology Process of 5-Fhdpat

There total 9 articles about 5-Fhdpat 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 8 steps
1: Tl(NO3)3 / methanol
2: aq. HCl / diethyl ether
3: benzene
4: NaCNBH3 / methanol
6: H2 / Pd/C / methanol
7: K2CO3 / acetonitrile
8: 48percent HBr / 120 °C
With hydrogenchloride; hydrogen bromide; hydrogen; sodium cyanoborohydride; potassium carbonate; thallium(III) nitrate; palladium on activated charcoal; In methanol; diethyl ether; acetonitrile; benzene;
DOI:10.1021/jm00168a002
Guidance literature:
Multi-step reaction with 9 steps
1: dimethylsulfoxide
2: Tl(NO3)3 / methanol
3: aq. HCl / diethyl ether
4: benzene
5: NaCNBH3 / methanol
7: H2 / Pd/C / methanol
8: K2CO3 / acetonitrile
9: 48percent HBr / 120 °C
With hydrogenchloride; hydrogen bromide; hydrogen; sodium cyanoborohydride; potassium carbonate; thallium(III) nitrate; palladium on activated charcoal; In methanol; diethyl ether; dimethyl sulfoxide; acetonitrile; benzene;
DOI:10.1021/jm00168a002
Guidance literature:
Multi-step reaction with 6 steps
1: benzene
2: NaCNBH3 / methanol
4: H2 / Pd/C / methanol
5: K2CO3 / acetonitrile
6: 48percent HBr / 120 °C
With hydrogen bromide; hydrogen; sodium cyanoborohydride; potassium carbonate; palladium on activated charcoal; In methanol; acetonitrile; benzene;
DOI:10.1021/jm00168a002
Refernces Edit
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