103-32-2 | N-Phenylbenzylamine

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$14.00	$10.00
25g	98%	in stock	$44.00	$31.00
100g	98%	in stock	$84.00	$59.00

Description

• Catalog Number: AB46689
• Chemical Name: N-Phenylbenzylamine
• CAS Number: 103-32-2
• Molecular Formula: C13H13N
• Molecular Weight: 183.249
• MDL Number: MFCD00003018
• SMILES: c1ccc(cc1)NCc1ccccc1
• NSC Number: 147284

Computed Properties

• Complexity: 143
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 3.1

Upstream Synthesis Route

N-Benzylaniline is a versatile compound widely used in chemical synthesis as a key building block in various reactions. Its primary application lies in organic synthesis processes where it serves as a valuable intermediate to create a wide range of other important compounds. With its unique structure and reactivity, N-Benzylaniline plays a crucial role in the production of pharmaceuticals, agrochemicals, and materials science. Whether it is forming complex organic molecules or facilitating the synthesis of new compounds, N-Benzylaniline proves to be an essential component in the realm of chemical synthesis.

Literature

• 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