Home Indole and Oxindoles 4770-03-0
4770-03-0,MFCD13178651
Catalog No.:AA006ZNX

4770-03-0 | 3-Nitro-1H-indole

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100mg
98%
in stock  
$17.00   $12.00
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250mg
98%
in stock  
$33.00   $23.00
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1g
95%
in stock  
$93.00   $65.00
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5g
96%
in stock  
$333.00   $233.00
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10g
98%
in stock  
$429.00   $301.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA006ZNX
Chemical Name:
3-Nitro-1H-indole
CAS Number:
4770-03-0
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.1454
MDL Number:
MFCD13178651
SMILES:
[O-][N+](=O)c1c[nH]c2c1cccc2
Properties
Computed Properties
 
Complexity:
190  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.4  

Downstream Synthesis Route

[1]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1904,vol.<5>13I,p.242    GazzettaChimicaItaliana,1904,vol.34II,p.60

[1]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1904,vol.<5>13I,p.242    GazzettaChimicaItaliana,1904,vol.34II,p.60

[1]GazzettaChimicaItaliana,1904,vol.34II,p.65,66

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1997,vol.36,p.1071-1073

[2]TetrahedronLetters,2011,vol.52,p.5081-5082

[3]LettersinOrganicChemistry,2015,vol.12,p.136-140

[4]SyntheticCommunications,2018,vol.48,p.59-67

[5]TetrahedronLetters,2012,vol.53,p.4841-4842

[6]InternationalJournalofChemicalKinetics,2017,vol.49,p.622-632

[7]BioorganicandMedicinalChemistry,2007,vol.15,p.3248-3265

[8]Patent:US2013/102576,2013,A1.Locationinpatent:Paragraph0434

[9]Patent:WO2013/57013,2013,A2.Locationinpatent:Page/Pagecolumn96;97

[10]AdvancedSynthesisandCatalysis,2019,vol.361,p.2255-2261

[11]Tetrahedron,2000,vol.56,p.10133-10140

[12]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1984,vol.23,p.930-933

[13]Patent:WO2017/35351,2017,A1.Locationinpatent:Paragraph0509;0510

[14]Patent:WO2017/35349,2017,A1.Locationinpatent:Paragraph0512

[15]AngewandteChemie-InternationalEdition,2018,vol.57,p.2134-2138    Angew.Chem.,2018,vol.130,p.2156-2160,5

[16]AngewandteChemie-InternationalEdition,2019,vol.58,p.5422-5426    Angew.Chem.,2019,vol.131,p.5476-5480,5

[17]TetrahedronLetters,2019,vol.60,p.1885-1890

[1]ChemicalandPharmaceuticalBulletin,1987,vol.35,p.2656-2660

[2]ChemicalandPharmaceuticalBulletin,1987,vol.35,p.2656-2660

[3]ChemicalandPharmaceuticalBulletin,1987,vol.35,p.2656-2660

Literature

Title: Multicomponent domino [4+2]/[3+2] cycloadditions of nitroheteroaromatics: an efficient synthesis of fused nitrogenated polycycles.

Journal: Organic letters 20071011

Title: Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors.

Journal: Chirality 20051101

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