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Home Fluorides 387-43-9
387-43-9,MFCD11656134
Catalog No.:AA0037UR

387-43-9 | 4-Fluoroindole

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$21.00   $15.00
- +
10g
98%
in stock  
$38.00   $27.00
- +
25g
98%
in stock  
$77.00   $54.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0037UR
Chemical Name:
4-Fluoroindole
CAS Number:
387-43-9
Molecular Formula:
C8H6FN
Molecular Weight:
135.1383
MDL Number:
MFCD11656134
SMILES:
Fc1cccc2c1cc[nH]2
Properties
Computed Properties
 
Complexity:
126  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.8  

Upstream Synthesis Route

[1]Patent:WO2009/130481,2009,A1,.Locationinpatent:Page/Pagecolumn149-150

[2]Patent:JP2016/204312,2016,A,.Locationinpatent:Paragraph0026;0071;0076;0079;0085

[1]OrganicandBiomolecularChemistry,2004,vol.2,#2,p.160-167

[2]JournaloftheChemicalSociety,1955,p.1283,1284

[3]Patent:JP2016/204312,2016,A,

[4]Patent:JP2016/204312,2016,A,

[5]Patent:WO2009/130481,2009,A1,

[1]EuropeanJournalofOrganicChemistry,2006,#13,p.2956-2969

[1]CanadianJournalofChemistry,2007,vol.85,#4,p.283-292

[2]Nucleosides,NucleotidesandNucleicAcids,2007,vol.26,#8-9,p.869-871

[3]JournaloftheChemicalSociety,1955,p.1283,1284

[1]GreenChemistry,2012,vol.14,#5,p.1281-1283

Downstream Synthesis Route

[1]CanadianJournalofChemistry,2007,vol.85,p.283-292

[2]Nucleosides,nucleotidesandnucleicacids,2007,vol.26,p.869-871

[3]JournaloftheChemicalSociety,1955,p.1283,1284

[1]JournalofHeterocyclicChemistry,1987,vol.24,p.1499-1501

[1]BioorganicandMedicinalChemistry,2014,vol.22,p.1649-1666

[2]Patent:WO2016/86200,2016,A1.Locationinpatent:Page/Pagecolumn343

[3]ACSMedicinalChemistryLetters,2013,vol.4,p.964-968

[4]Patent:WO2011/119663,2011,A1.Locationinpatent:Page/Pagecolumn187-188

[5]Patent:WO2015/56180,2015,A1.Locationinpatent:Page/Pagecolumn67;68

[6]Patent:WO2009/130481,2009,A1.Locationinpatent:Page/Pagecolumn149

[7]BioorganicandMedicinalChemistryLetters,2002,vol.12,p.3105-3109

[8]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.3287-3291

[9]Patent:US2008/27122,2008,A1.Locationinpatent:Page/Pagecolumn11

[10]Patent:WO2005/66165,2005,A1.Locationinpatent:Page/Pagecolumn112-113

[11]JournalofMedicinalChemistry,2011,vol.54,p.166-178

[12]Patent:WO2015/66344,2015,A1.Locationinpatent:Page/Pagecolumn196

[13]Patent:WO2017/153952,2017,A1.Locationinpatent:Page/Pagecolumn151

[14]JournalofOrganicChemistry,2018,vol.83,p.2425-2437

[1]BioorganicandMedicinalChemistryLetters,2014,vol.24,p.4754-4758

[2]Patent:US2007/249624,2007,A1.Locationinpatent:Page/Pagecolumn11;18

[3]BioorganicandMedicinalChemistryLetters,2003,vol.13,p.2261-2267

[4]JournalofMedicinalChemistry,2003,vol.46,p.4236-4239

[5]OrganicandBiomolecularChemistry,2005,vol.3,p.1781-1786

3-fluoro-trans-2-β-(dimethylamino)vinylnitrobenzene 
  387-43-9 

[1]OrganicandBiomolecularChemistry,2004,vol.2,p.160-167

[2]Patent:WO2009/49113,2009,A1.Locationinpatent:Page/Pagecolumn19

Literature

Title: Prediction of genotoxicity of chemical compounds by statistical learning methods.

Journal: Chemical research in toxicology 20050601

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SDS
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