CAS 17480-69-2 | S-(-)-N-Benzyl-1-phenylethylamine | CAS Number 17480-69-2

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17480-69-2 | S-(-)-N-Benzyl-1-phenylethylamine

CAS No: 17480-69-2 Catalog No: AG003CEE MDL No:MFCD00066325

Product Description

Catalog Number:

AG003CEE

Chemical Name:

S-(-)-N-Benzyl-1-phenylethylamine

CAS Number:

17480-69-2

Molecular Formula:

C15H17N

Molecular Weight:

211.3022

MDL Number:

MFCD00066325

IUPAC Name:

(1S)-N-benzyl-1-phenylethanamine

InChI:

InChI=1S/C15H17N/c1-13(15-10-6-3-7-11-15)16-12-14-8-4-2-5-9-14/h2-11,13,16H,12H2,1H3/t13-/m0/s1

InChI Key:

ZYZHMSJNPCYUTB-ZDUSSCGKSA-N

SMILES:

C[C@@H](c1ccccc1)NCc1ccccc1

Properties

Complexity:

178

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

211.136g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

211.308g/mol

Monoisotopic Mass:

211.136g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

12A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

3.2

Literature

Title	Journal
On the origins of diastereoselectivity in the conjugate additions of the antipodes of lithium N-benzyl-(N-α-methylbenzyl)amide to enantiopure cis- and trans-dioxolane containing α,β-unsaturated esters.	Organic & biomolecular chemistry 20120814
Parallel kinetic resolution of tert-butyl (RS)-3-oxy-substituted cyclopent-1-ene-carboxylates for the asymmetric synthesis of 3-oxy-substituted cispentacin and transpentacin derivatives.	Organic & biomolecular chemistry 20080621
Asymmetric synthesis of vicinal amino alcohols: xestoaminol C, sphinganine and sphingosine.	Organic & biomolecular chemistry 20080507
Asymmetric synthesis of N,O,O,O-tetra-acetyl d-lyxo-phytosphingosine, jaspine B (pachastrissamine), 2-epi-jaspine B, and deoxoprosophylline via lithium amide conjugate addition.	Organic & biomolecular chemistry 20080507