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Home Indole and Oxindoles 4769-97-5
4769-97-5,MFCD00010056
Catalog No.:AA00341R

4769-97-5 | 4-Nitroindole

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Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$6.00   $4.00
- +
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$18.00   $13.00
- +
10g
98%
in stock  
$35.00   $25.00
- +
25g
98%
in stock  
$84.00   $59.00
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100g
98%
in stock  
$299.00   $210.00
- +
  • 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:
AA00341R
Chemical Name:
4-Nitroindole
CAS Number:
4769-97-5
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.1454
MDL Number:
MFCD00010056
SMILES:
[O-][N+](=O)c1cccc2c1cc[nH]2
Properties
Properties
 
BP:
362.6°C at 760 mmHg  
Form:
Solid  
MP:
205-207 °C(lit.)  
Refractive Index:
1.5770 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
190  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.6  

Upstream Synthesis Route

[1]Patent:US6255306,2001,B1,

[2]Chemistry-AEuropeanJournal,2014,vol.20,#11,p.3050-3060

[3]AdvancedSynthesisandCatalysis,2017,vol.359,#13,p.2280-2287

[4]RSCAdvances,2014,vol.4,#43,p.22567-22574

[5]ChemicalandPharmaceuticalBulletin,1981,vol.29,#3,p.726-738

[6]EuropeanJournalofMedicinalChemistry,2017,vol.134,p.13-23

[7]JournalofMedicinalChemistry,2002,vol.45,#19,p.4128-4139

[8]JournaloftheAmericanChemicalSociety,2017,vol.139,#20,p.7004-7011

[9]Patent:WO2009/34581,2009,A1,.Locationinpatent:Page/Pagecolumn24

[10]Patent:WO2011/23081,2011,A1,.Locationinpatent:Page/Pagecolumn55-56

[11]Patent:WO2012/28106,2012,A1,.Locationinpatent:Page/Pagecolumn50

[12]ACSCatalysis,2014,vol.4,#5,p.1441-1450

[13]RSCAdvances,2016,vol.6,#63,p.58805-58812

[14]CatalysisScienceandTechnology,2018,vol.8,#5,p.1454-1467

[1]Patent:US6162818,2000,A,

[1]ChemicalandPharmaceuticalBulletin,1981,vol.29,#3,p.726-738

[2]ChemicalandPharmaceuticalBulletin,1981,vol.29,#3,p.726-738

[3]ChemicalandPharmaceuticalBulletin,1981,vol.29,#3,p.726-738

[1]JournalofOrganicChemistryUSSR(EnglishTranslation),1983,p.2117-2120

[2]ZhurnalOrganicheskoiKhimii,1983,vol.19,#11,p.2420-2423

[3]JournalofOrganicChemistryUSSR(EnglishTranslation),1983,p.2117-2120

[4]ZhurnalOrganicheskoiKhimii,1983,vol.19,#11,p.2420-2423

[1]JournalofMedicinalChemistry,2011,vol.54,#1,p.166-178

Downstream Synthesis Route

[1]Tetrahedron,1990,vol.46,p.6113-6124

[1]Somei;Tsuchiya[ChemicalandPharmaceuticalBulletin,1981,vol.29,#11,p.3145-3157]

[2]Halaiev,Olexandr;Garazd,Myroslav;Gzella,Andrzej;Lesyk,Roman[TetrahedronLetters,2017,vol.58,#13,p.1324-1325]

[3]Iqbal,SaqibA.;Cid,Jessica;Procter,RichardJ.;Uzelac,Marina;Yuan,Kang;Ingleson,MichaelJ.[AngewandteChemie-InternationalEdition,2019,vol.58,#43,p.15381-15385][Angew.Chem.,2019,vol.131,p.15525-15529,5]

[1]Prueger,Birgit;Bach,Thorsten[Synthesis,2007,#7,p.1103-1106]

[2]CurrentPatentAssignee:RUTGERS,THESTATEUNIVERSITYOFNEWJERSEY-WO2020/150446,2020,A1Locationinpatent:Paragraph0494-0495

[3]Bergman,Jan;Sand,Peter[Tetrahedron,1990,vol.46,#17,p.6085-6112]

[4]Lee,Sanghee;Park,SeungBum[OrganicLetters,2009,vol.11,#22,p.5214-5217]

[5]Lee,Sanghee;Jo,Ala;Park,SeungBum[MedChemComm,2013,vol.4,#1,p.228-232]

[1]Somei;Tsuchiya[ChemicalandPharmaceuticalBulletin,1981,vol.29,#11,p.3145-3157]

[2]Wang,Xi;Xu,Yan;Mo,Fanyang;Ji,Guojing;Qiu,Di;Feng,Jiajie;Ye,Yuxuan;Zhang,Songnan;Zhang,Yan;Wang,Jianbo[JournaloftheAmericanChemicalSociety,2013,vol.135,#28,p.10330-10333]

[3]Locationinpatent:experimentalpartTanaka,Minoru;Hikawa,Hidemasa;Yokoyama,Yuusaku[Tetrahedron,2011,vol.67,#33,p.5897-5901]

[1]JournalofMedicinalChemistry,2004,vol.47,p.871-887

[2]TetrahedronLetters,2017,vol.58,p.1324-1325

[3]JournalofMedicinalChemistry,2005,vol.48,p.3417-3427

[4]Patent:US2009/227575,2009,A1.Locationinpatent:Page/Pagecolumn21

[5]JournalofMedicinalChemistry,1993,vol.36,p.1104-1107

[6]JournalofMedicinalChemistry,1992,vol.35,p.177-184

[7]Patent:US6521658,2003,B1

[8]AdvancedSynthesisandCatalysis,2015,vol.357,p.355-360

Literature

Title: Modes of action of microbially-produced phytotoxins.

Journal: Toxins 20110801

Title: The thaxtomin phytotoxins: sources, synthesis, biosynthesis, biotransformation and biological activity.

Journal: Phytochemistry 20090501

Title: Influence of thaxtomins in different combinations and concentrations on growth of micropropagated potato shoot cultures.

Journal: Journal of agricultural and food chemistry 20060503

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