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60434-13-1,MFCD02956479
Catalog No.:AA00EIA9

60434-13-1 | 5-Chloro-1-methyl-1h-indole-2,3-dione

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$29.00   $21.00
- +
1g
98%
in stock  
$67.00   $47.00
- +
5g
98%
in stock  
$116.00   $82.00
- +
  • 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:
AA00EIA9
Chemical Name:
5-Chloro-1-methyl-1h-indole-2,3-dione
CAS Number:
60434-13-1
Molecular Formula:
C9H6ClNO2
Molecular Weight:
195.6024
MDL Number:
MFCD02956479
SMILES:
Clc1ccc2c(c1)C(=O)C(=O)N2C
Properties
Computed Properties
 
Complexity:
266  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
XLogP3:
1.2  

Upstream Synthesis Route

[1]RSCAdvances,2015,vol.5,#125,p.103280-103283

[2]TetrahedronLetters,2016,vol.57,#1,p.39-42

[3]Synlett,2016,vol.27,#8,p.1292-1296

[4]JournaloftheAmericanChemicalSociety,2010,vol.132,#26,p.8900-8902

[5]Chemistry-AEuropeanJournal,2007,vol.13,#4,p.1032-1046

[1]JournalofHeterocyclicChemistry,2008,vol.45,#4,p.969-973

[2]OrganicLetters,2017,vol.19,#12,p.3119-3122

[3]MedicinalChemistryResearch,2007,vol.15,#9,p.492-510

[4]JournalofOrganicChemistry,2017,vol.82,#16,p.8548-8567

[5]TetrahedronLetters,2015,vol.56,#51,p.7074-7081

[6]AngewandteChemie-InternationalEdition,2006,vol.45,#20,p.3353-3356

[7]ChemicalCommunications,2017,vol.53,#10,p.1684-1687

[8]BioorganicandMedicinalChemistryLetters,2002,vol.12,#17,p.2427-2430

[9]EuropeanJournalofMedicinalChemistry,2010,vol.45,#3,p.1068-1077

[10]JournaloftheAmericanChemicalSociety,2010,vol.132,#43,p.15328-15333

[11]GreenChemistry,2011,vol.13,#9,p.2553-2560

[12]Synlett,2011,#15,p.2256-2258

[13]EuropeanJournalofOrganicChemistry,2012,#12,p.2359-2366

[14]Chemistry-AEuropeanJournal,2012,vol.18,#31,p.9645-9650

[15]Synlett,2012,vol.23,#15,p.2274-2278

[16]Chemistry-AnAsianJournal,2012,vol.7,#10,p.2446-2449,4

[17]Chemistry-AnAsianJournal,2012,vol.7,#10,p.2446-2449

[18]AngewandteChemie-InternationalEdition,2013,vol.52,#41,p.10780-10783

[19]Angew.Chem.,2013,vol.125,#41,p.10980-10983

[20]Chemistry-AEuropeanJournal,2014,vol.20,#20,p.5905-5909

[21]Chemistry-AEuropeanJournal,2016,vol.22,#8,p.2595-2598

[22]OrganicLetters,2014,vol.16,#12,p.3192-3195

[23]JournalofEnzymeInhibitionandMedicinalChemistry,2014,vol.29,#4,p.457-468

[24]JournalofOrganicChemistry,2014,vol.79,#22,p.11161-11169

[25]EuropeanJournalofMedicinalChemistry,2015,vol.102,p.413-424

[26]OrganicLetters,2016,vol.18,#20,p.5232-5235

[27]JournalofOrganicChemistry,2016,vol.81,#20,p.9757-9764

[28]AdvancedSynthesisandCatalysis,2017,vol.359,#1,p.49-57

[29]TetrahedronLetters,2017,vol.58,#27,p.2636-2639

[30]AdvancedSynthesisandCatalysis,2017,vol.359,#22,p.3934-3939

[31]JournalofOrganicChemistry,2017,vol.82,#19,p.10121-10128

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

[33]JournalofFluorineChemistry,2018,vol.215,p.44-51

[34]JournalofOrganicChemistry,2018,

[35]EuropeanJournalofMedicinalChemistry,2019,p.147-160

[1]Synlett,2017,vol.28,#17,p.2307-2310

[2]Synlett,2018,vol.29,#2,p.215-218

[1]Patent:CN104059012,2016,B,.Locationinpatent:Paragraph0033-0035;0048;0054;0059;0063

[2]OrganicandBiomolecularChemistry,2014,vol.12,#21,p.3349-3353

[1]EuropeanJournalofOrganicChemistry,2018,vol.2018,#22,p.2762-2767

[2]EuropeanJournalofOrganicChemistry,2016,vol.2016,#12,p.2105-2109

[3]Synthesis(Germany),2015,vol.47,#13,p.1937-1943

[4]TetrahedronLetters,2017,vol.58,#49,p.4591-4594

[5]ACSCatalysis,2016,vol.6,#10,p.6853-6860

[6]Synlett,2018,vol.29,#7,p.969-973

Downstream Synthesis Route

[1]JournalofHeterocyclicChemistry,2008,vol.45,p.969-973

[2]OrganicLetters,2017,vol.19,p.3119-3122

[3]MedicinalChemistryResearch,2007,vol.15,p.492-510

[4]JournalofOrganicChemistry,2017,vol.82,p.8548-8567

[5]TetrahedronLetters,2015,vol.56,p.7074-7081

[6]AngewandteChemie-InternationalEdition,2006,vol.45,p.3353-3356

[7]ChemicalCommunications,2017,vol.53,p.1684-1687

[8]JournalofOrganicChemistry,2019,vol.84,p.4000-4008

[9]BioorganicandMedicinalChemistryLetters,2002,vol.12,p.2427-2430

[10]EuropeanJournalofMedicinalChemistry,2010,vol.45,p.1068-1077

[11]JournaloftheAmericanChemicalSociety,2010,vol.132,p.15328-15333

[12]GreenChemistry,2011,vol.13,p.2553-2560

[13]Synlett,2011,p.2256-2258

[14]EuropeanJournalofOrganicChemistry,2012,p.2359-2366

[15]Chemistry-AEuropeanJournal,2012,vol.18,p.9645-9650

[16]Synlett,2012,vol.23,p.2274-2278

[17]AngewandteChemie-InternationalEdition,2013,vol.52,p.10780-10783    Angew.Chem.,2013,vol.125,p.10980-10983

[18]Chemistry-AEuropeanJournal,2014,vol.20,p.5905-5909

[19]OrganicLetters,2014,vol.16,p.3192-3195

[20]JournalofEnzymeInhibitionandMedicinalChemistry,2014,vol.29,p.457-468

[21]JournalofOrganicChemistry,2014,vol.79,p.11161-11169

[22]EuropeanJournalofMedicinalChemistry,2015,vol.102,p.413-424

[23]OrganicLetters,2016,vol.18,p.5232-5235

[24]JournalofOrganicChemistry,2016,vol.81,p.9757-9764

[25]AdvancedSynthesisandCatalysis,2017,vol.359,p.49-57

[26]TetrahedronLetters,2017,vol.58,p.2636-2639

[27]AdvancedSynthesisandCatalysis,2017,vol.359,p.3934-3939

[28]JournalofOrganicChemistry,2017,vol.82,p.10121-10128

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

[30]JournalofFluorineChemistry,2018,vol.215,p.44-51

[31]JournalofOrganicChemistry,2018,vol.83,p.14102-14109

[32]EuropeanJournalofMedicinalChemistry,2019,vol.162,p.147-160

[33]JournalofOrganometallicChemistry,2019,vol.896,p.1-4

[34]AngewandteChemie-InternationalEdition,2019,vol.58,p.13335-13339    Angew.Chem.,2019,vol.131,p.13469-13473,5

[35]Metabolites,2020,vol.10

[36]Chemistry-AnAsianJournal,2012,vol.7,p.2446-2449,4

60434-13-1    81290-20-2   
5-chloro-3-hydroxy-1-methyl-3-(trifluoromethyl)indolin-2-one 

[1]JournalofHeterocyclicChemistry,2008,vol.45,p.969-973

[2]MonatsheftefurChemie,2017,vol.148,p.757-764

[3]MedicinalChemistryResearch,2007,vol.15,p.492-510

[1]RSCAdvances,2015,vol.5,p.103280-103283

[2]TetrahedronLetters,2016,vol.57,p.39-42

[3]Synlett,2016,vol.27,p.1292-1296

[4]JournaloftheAmericanChemicalSociety,2010,vol.132,p.8900-8902

[5]Chemistry-AEuropeanJournal,2007,vol.13,p.1032-1046

60-27-5    60434-13-1   
C13H13ClN4O3 

[1]BioorganicandMedicinalChemistryLetters,2010,vol.20,p.4468-4471

[1]AngewandteChemie-InternationalEdition,2014,vol.53,p.9582-9586,5    Angew.Chem.,2014,vol.126,p.9736-9740,5    AngewandteChemie,2014,vol.126,p.9736-9740,5

[2]Tetrahedron,2011,vol.67,p.982-989

[3]OrganicLetters,2015,vol.17,p.1373-1376

[4]Chemistry-AEuropeanJournal,2016,vol.22,p.2595-2598

[5]OrganicLetters,2016,vol.18,p.5232-5235

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

[7]JournalofFluorineChemistry,2018,vol.215,p.44-51

[8]Synlett,2019,vol.30,p.1067-1072

[9]Organicandbiomolecularchemistry,2020,vol.18,p.3843-3847

Literature

Title: Chemical synthesis, in vitro acetohydroxyacid synthase (AHAS) inhibition, herbicidal activity, and computational studies of isatin derivatives.

Journal: Journal of agricultural and food chemistry 20110928

Title: Design, synthesis, and evaluation of nonpeptidic inhibitors of human rhinovirus 3C protease.

Journal: Journal of medicinal chemistry 19961220

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