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N-Phenylbenzylamine

CAS No.:
103-32-2
Catalog Number:
AG0035C9
Molecular Formula:
C13H13N
Molecular Weight:
183.2490
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25g
98%
In Stock USA
United States
$32
- +
100g
98%
In Stock USA
United States
$94
- +
500g
98%
In Stock USA
United States
$400
- +
Product Description
Catalog Number:
AG0035C9
Chemical Name:
N-Phenylbenzylamine
CAS Number:
103-32-2
Molecular Formula:
C13H13N
Molecular Weight:
183.2490
MDL Number:
MFCD00003018
IUPAC Name:
N-benzylaniline
InChI:
InChI=1S/C13H13N/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13/h1-10,14H,11H2
InChI Key:
GTWJETSWSUWSEJ-UHFFFAOYSA-N
SMILES:
c1ccc(cc1)NCc1ccccc1
EC Number:
203-100-4
UNII:
R1FVH9A316
NSC Number:
147284
Properties
Complexity:
143  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
183.105g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
183.254g/mol
Monoisotopic Mass:
183.105g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
12A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1  
Literature
Title Journal
Dissociative benzyl cation transfer versus proton transfer: loss of benzene from protonated N-benzylaniline. The Journal of organic chemistry 20120817
Synthesis and structure-activity relationships of a class of sodium iodide symporter function inhibitors. ChemMedChem 20111004
N-Benzyl-aniline. Acta crystallographica. Section E, Structure reports online 20110501
Redetermination of 1-benzyl-3-furoyl-1-phenyl-thio-urea. Acta crystallographica. Section E, Structure reports online 20090301
Synthesis, characterization and catalytic activity of saturated and unsaturated N-heterocyclic carbene iridium(i) complexes. Dalton transactions (Cambridge, England : 2003) 20090207
Anti-microtubule activity of tubeimoside I and its colchicine binding site of tubulin. Cancer chemotherapy and pharmacology 20080901
de novo design and synthesis of N-benzylanilines as new candidates for VEGFR tyrosine kinase inhibitors. Organic & biomolecular chemistry 20080321
Optically sensed, molecular shuttles driven by acid-base chemistry. Chemical communications (Cambridge, England) 20071207
Discovery of small molecule CXCR4 antagonists. Journal of medicinal chemistry 20071115
Copper-catalyzed amidation of sp3 C-H bonds adjacent to a nitrogen atom. Organic letters 20070913
Optical properties of the poly(N-benzylaniline) thin film. The journal of physical chemistry. B 20060112
[2]pseudorotaxane formation with N-benzylanilinium axles and 24-crown-8 ether wheels. Organic letters 20051027
N-benzylideneaniline and N-benzylaniline are potent inhibitors of lignostilbene-alpha,beta-dioxygenase, a key enzyme in oxidative cleavage of the central double bond of lignostilbene. Journal of enzyme inhibition and medicinal chemistry 20030601
Synthesis, anticancer activity, and inhibition of tubulin polymerization by conformationally restricted analogues of lavendustin A. Journal of medicinal chemistry 20030424
A new pathway for hydroamination. Mechanism of palladium-catalyzed addition of anilines to vinylarenes. Journal of the American Chemical Society 20020220
Antidepressant activity of aspartic acid derivatives. Bulletin of experimental biology and medicine 20010401
Properties