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Home Amines 2637-31-2
2637-31-2,MFCD00778682
Catalog No.:AA002SU3

2637-31-2 | 3-(3,4-Dihydroquinolin-1(2h)-yl)propan-1-amine

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1g
95%
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$172.00   $120.00
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5g
95%
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$685.00   $479.00
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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:
AA002SU3
Chemical Name:
3-(3,4-Dihydroquinolin-1(2h)-yl)propan-1-amine
CAS Number:
2637-31-2
Molecular Formula:
C12H18N2
Molecular Weight:
190.2847
MDL Number:
MFCD00778682
SMILES:
NCCCN1CCCc2c1cccc2
Properties
Computed Properties
 
Complexity:
170  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
1.9  

Downstream Synthesis Route

[1]Whitmoreetal.[JournaloftheAmericanChemicalSociety,1944,vol.66,p.725,728]

2637-31-2   
2-1-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-propyl-1,3dithiolane-2-carboxylicacidethylester 
 
((S)-1-{1-3-(3,4-Dihydro-2H-quinolin-1-yl)-propylaminooxalyl-propylcarbamoyl}-3-methyl-butyl)-carbamicacidbenzylester 

[1]Li,Zhaozhao;Ortega-Vilain,Anne-Cécile;Patil,GirishS.;Chu,Der-Lun;Foreman;Eveleth,DavidD.;Powers,JamesC.[JournalofMedicinalChemistry,1996,vol.39,#20,p.4089-4098]

2637-31-2   
2-1-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-2-phenyl-ethyl-1,3dithiolane-2-carboxylicacidethylester 
 
((S)-1-{1-Benzyl-2-3-(3,4-dihydro-2H-quinolin-1-yl)-propylcarbamoyl-2-oxo-ethylcarbamoyl}-3-methyl-butyl)-carbamicacidbenzylester 

[1]Li,Zhaozhao;Ortega-Vilain,Anne-Cécile;Patil,GirishS.;Chu,Der-Lun;Foreman;Eveleth,DavidD.;Powers,JamesC.[JournalofMedicinalChemistry,1996,vol.39,#20,p.4089-4098]

[1]Okimoto,Mitsuhiro;Yoshida,Takashi;Hoshi,Masayuki;Hattori,Kazuyuki;Komata,Masashi;Numata,Kaori;Tomozawa,Kenta[AustralianJournalofChemistry,2007,vol.60,#4,p.236-242]

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

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