Home Indole and Oxindoles 103549-24-2
103549-24-2,MFCD00716928
Catalog No.:AA0085JY

103549-24-2 | tert-butyl N-[2-(1H-indol-3-yl)ethyl]carbamate

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100mg
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250mg
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1g
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5g
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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:
AA0085JY
Chemical Name:
tert-butyl N-[2-(1H-indol-3-yl)ethyl]carbamate
CAS Number:
103549-24-2
Molecular Formula:
C15H20N2O2
Molecular Weight:
260.3315
MDL Number:
MFCD00716928
SMILES:
O=C(OC(C)(C)C)NCCc1c[nH]c2c1cccc2
Properties
Computed Properties
 
Complexity:
312  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
3.2  

Downstream Synthesis Route
103549-24-2    5332-06-9   
1,1-dimethylethyl2-1-(3-cyanopropyl)-1H-indol-3-ylethylcarbamate 

[1]TetrahedronLetters,2015,vol.56,p.6012-6015

[2]Synthesis,2006,p.3948-3954

55854-46-1    103549-24-2   
C19H21BrN2O4S2 

[1]JournalofMedicinalChemistry,2007,vol.50,p.5535-5538

113860-02-9    103549-24-2   
{(η5-C5Me5)(η6-N(b)-BOC-tryptophane)ruthenium}OTf 

[1]Lomenzo,StaceyA.;Nolan,StevenP.;Trudell,MarkL.[Organometallics,1994,vol.13,#2,p.676-681]

[1]AdvancedSynthesisandCatalysis,2014,vol.356,p.3377-3382

[2]OrganicandBiomolecularChemistry,2009,vol.7,p.1388-1396

[3]OrganicLetters,2013,vol.15,p.4338-4341

[1]OrganicandBiomolecularChemistry,2009,vol.7,p.1388-1396

Literature

Title: Synthesis of azepino[4,5-b]indolones via an intermolecular radical oxidative substitution of N-Boc tryptamine.

Journal: Organic & biomolecular chemistry 20090407

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SDS
Tags:103549-24-2 Molecular Formula|103549-24-2 MDL|103549-24-2 SMILES|103549-24-2 tert-butyl N-[2-(1H-indol-3-yl)ethyl]carbamate