Home Amines 13324-66-8
13324-66-8,MFCD00089909
Catalog No.:AA0014DE

13324-66-8 | N-Cyclopropylbenzylamine

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100mg
98%
in stock  
$8.00   $6.00
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250mg
98%
in stock  
$13.00   $9.00
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1g
98%
in stock  
$45.00   $32.00
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5g
98%
in stock  
$100.00   $70.00
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25g
98%
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$473.00   $331.00
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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:
AA0014DE
Chemical Name:
N-Cyclopropylbenzylamine
CAS Number:
13324-66-8
Molecular Formula:
C10H13N
Molecular Weight:
147.2169
MDL Number:
MFCD00089909
SMILES:
N(C1CC1)Cc1ccccc1
Properties
Computed Properties
 
Complexity:
112  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2.1  

Downstream Synthesis Route

[1]JournalofOrganicChemistry,2016,vol.81,p.4235-4243

[2]Journalofmedicinalchemistry,1973,vol.16,p.101-106

[1]JournalofMedicinalChemistry,1984,vol.27,p.1335-1339

[2]JournalofOrganicChemistry,2000,vol.65,p.96-103

[3]BioorganicandMedicinalChemistry,2006,vol.14,p.8506-8518

[1]JournaloftheChemicalSociety.PerkintransactionsI,1984,p.147-153

[1]JournalofMedicinalChemistry,1984,vol.27,p.1335-1339

[2]Tetrahedron,2001,vol.57,p.4507-4522

[3]SyntheticCommunications,2003,vol.33,p.3419-3425

[4]Phosphorus,SulfurandSiliconandtheRelatedElements,2015,vol.190,p.1127-1137

[1]JournalofHeterocyclicChemistry,1983,vol.20,p.1031-1036

Literature

Title: Predicting biological functions of compounds based on chemical-chemical interactions.

Journal: PloS one 20110101

Title: Cytochrome P450-catalyzed oxidation of N-benzyl-N-cyclopropylamine generates both cyclopropanone hydrate and 3-hydroxypropionaldehyde via hydrogen abstraction, not single electron transfer.

Journal: Journal of the American Chemical Society 20060315

Title: Cyclopropylamine inactivation of cytochromes P450: role of metabolic intermediate complexes.

Journal: Archives of biochemistry and biophysics 20050415

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SDS
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