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52537-00-5,MFCD07371639
Catalog No.:AA003N2L

52537-00-5 | 6-Chloro-2,3-dihydro-1H-indole

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Purity
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Price(USD)
Quantity
  
100mg
95%
in stock  
$26.00   $18.00
- +
250mg
95%
in stock  
$33.00   $23.00
- +
1g
95%
in stock  
$125.00   $88.00
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5g
95%
in stock  
$500.00   $350.00
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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:
AA003N2L
Chemical Name:
6-Chloro-2,3-dihydro-1H-indole
CAS Number:
52537-00-5
Molecular Formula:
C8H8ClN
Molecular Weight:
153.6088
MDL Number:
MFCD07371639
SMILES:
Clc1ccc2c(c1)NCC2
NSC Number:
87628
Properties
Properties
 
BP:
250.3°C at 760 mmHg  
Form:
Solid  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
126  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.7  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,1990,vol.55,#2,p.580-584

[2]AdvancedSynthesisandCatalysis,2017,vol.359,#14,p.2358-2363

[3]ACSCatalysis,2018,vol.8,#2,p.1192-1196

[4]Organometallics,2018,vol.37,#4,p.584-591

[5]JournalofOrganicChemistry,1990,vol.55,#2,p.580-584

[1]JournaloftheAmericanChemicalSociety,1981,vol.103,#6,p.1525-1533

[1]JournaloftheAmericanChemicalSociety,1981,vol.103,#6,p.1525-1533

[1]TetrahedronLetters,2017,vol.58,#18,p.1747-1750

[1]Patent:WO2003/76398,2003,A2,.Locationinpatent:Page/Pagecolumn41

[2]Patent:US2011/21500,2011,A1,.Locationinpatent:Page/Pagecolumn49

[3]Patent:JP2015/193573,2015,A,.Locationinpatent:Paragraph0043

[4]Patent:WO2012/143726,2012,A1,.Locationinpatent:Page/Pagecolumn129

[5]JournalofMedicinalChemistry,2015,vol.58,#16,p.6574-6588

[6]Patent:WO2004/18414,2004,A2,.Locationinpatent:Page92

[7]BioorganicandMedicinalChemistryLetters,2002,vol.12,#21,p.3105-3109

[8]Patent:US2004/266843,2004,A1,.Locationinpatent:Page22

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

[10]ACSMedicinalChemistryLetters,2012,vol.3,#5,p.373-377

[11]Chemistry-AEuropeanJournal,2014,vol.20,#1,p.58-63

[12]JournalofOrganicChemistry,2016,vol.81,#2,p.396-403

[13]JournaloftheAmericanChemicalSociety,2016,vol.138,#37,p.12234-12242

[14]JournalofOrganicChemistry,2018,vol.83,#4,p.2425-2437

[15]OrganicandBiomolecularChemistry,2018,vol.16,#32,p.5889-5898

[16]OrganicandBiomolecularChemistry,2018,vol.16,#21,p.3889-3892

[17]Patent:US2008/81810,2008,A1,.Locationinpatent:Page/Pagecolumn67

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1990,vol.55,p.580-584

[2]AdvancedSynthesisandCatalysis,2017,vol.359,p.2358-2363

[3]ChemicalScience,2019,vol.10,p.4883-4889

[4]ACSCatalysis,2018,vol.8,p.1192-1196

[5]Organometallics,2018,vol.37,p.584-591

[6]JournalofOrganicChemistry,1990,vol.55,p.580-584

[1]JournaloftheAmericanChemicalSociety,1981,vol.103,p.1525-1533

[1]JournaloftheAmericanChemicalSociety,1981,vol.103,p.1525-1533

52537-00-5    333-20-0   
6-Chloro-5-thiocyanato-2,3-dihydro-1H-indole 

[1]JournalofMedicinalChemistry,1997,vol.40,p.3494-3496

52537-00-5    15268-31-2   
6-Chloro-1-(pyridin-3-ylcarbamoyl)indoline 

[1]JournalofMedicinalChemistry,1998,vol.41,p.1598-1612

[2]Patent:US5834494,1998,A

[3]BioorganicandMedicinalChemistry,1999,vol.7,p.2767-2773

Literature
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SDS
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