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Home Indole and Oxindoles 1127-59-9
1127-59-9,MFCD00022797
Catalog No.:AA007SAD

1127-59-9 | 7-Methyl-1H-indole-2,3-dione

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Purity
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Price(USD)
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250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$7.00   $5.00
- +
5g
97%
in stock  
$16.00   $11.00
- +
10g
97%
in stock  
$19.00   $14.00
- +
25g
97%
in stock  
$44.00   $31.00
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  • 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:
AA007SAD
Chemical Name:
7-Methyl-1H-indole-2,3-dione
CAS Number:
1127-59-9
Molecular Formula:
C9H7NO2
Molecular Weight:
161.1574
MDL Number:
MFCD00022797
SMILES:
O=C1Nc2c(C1=O)cccc2C
NSC Number:
3161
Properties
Computed Properties
 
Complexity:
237  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
XLogP3:
1.2  

Upstream Synthesis Route

[1]JournaloftheBrazilianChemicalSociety,2011,vol.22,#2,p.257-263

[1]EuropeanJournalofMedicinalChemistry,2016,vol.120,p.121-133

[1]ArchivderPharmazie(Weinheim,Germany),1929,p.583

[1]BioorganicandMedicinalChemistry,2015,vol.23,#14,p.3933-3937

[1]AngewandteChemie,1981,vol.93,#10,p.914-915

Downstream Synthesis Route
1127-59-9    593-08-8   
8-methyl-2-undecyl-quinoline-4-carboxylicacid 

[1]JournalofOrganicChemistry,1953,vol.18,p.1209,1219

[1]JournalofOrganicChemistry,2006,vol.71,p.5921-5929

[2]Patent:WO2014/169167,2014,A1.Locationinpatent:Page/Pagecolumn81

[3]BulletindelaSocieteChimiquedeFrance,1946,p.586,587

[4]JournalofMedicinalChemistry,2007,vol.50,p.21-39

[1]BioorganicandMedicinalChemistry,2005,vol.13,p.1945-1967

[2]HelveticaChimicaActa,1919,vol.2,p.239

[3]AnnalesdeChimie(Cachan,France),1926,vol.<10>5,p.326,350    ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1925,vol.181,p.792

[4]AttidellaAccademiaNazionaledeiLincei,ClassediScienzeFisiche,MatematicheeNaturali,Rendiconti,1955,vol.<8>18,p.647,653

[5]JournalofOrganicChemistry,1990,vol.55,p.560-564

[6]ChemischeBerichte,1992,vol.125,p.849-856

[7]ChineseJournalofChemistry,2012,vol.30,p.1748-1758

[8]ResearchonChemicalIntermediates,2013,vol.39,p.3071-3088

[9]MedicinalChemistryResearch,2014,vol.23,p.2161-2168

[10]Heterocycles,2014,vol.89,p.1923-1932

[11]BioorganicandMedicinalChemistry,2015,vol.23,p.3933-3937

[12]EuropeanJournalofMedicinalChemistry,2016,vol.120,p.121-133

[13]JournalofHeterocyclicChemistry,2016,vol.53,p.1036-1045

[14]OrganicLetters,2017,vol.19,p.646-649

[15]JournalofOrganicChemistry,2018,vol.83,p.7622-7632

[16]EuropeanJournalofMedicinalChemistry,2019,vol.163,p.840-852

[17]OrganicandBiomolecularChemistry,2019,vol.17,p.5099-5105

[1]Atwell;Baguley;Denny[JournalofMedicinalChemistry,1989,vol.32,#2,p.396-401]

[2]CurrentPatentAssignee:XENOVAGMBH-US4904659,1990,A

Literature

Title: A comprehensive strategy to discover inhibitors of the translesion synthesis DNA polymerase κ.

Journal: PloS one 20120101

Title: Selective inhibition of carboxylesterases by isatins, indole-2,3-diones.

Journal: Journal of medicinal chemistry 20070419

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

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SDS
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