23364-44-5 | (1S,2R)-(+)-2-Amino-1,2-diphenylethanol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$15.00	$10.00
5g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$45.00	$32.00
100g	98%	in stock	$140.00	$98.00
500g	98%	in stock	$643.00	$450.00

Description

• Catalog Number: AB22917
• Chemical Name: (1S,2R)-(+)-2-Amino-1,2-diphenylethanol
• CAS Number: 23364-44-5
• Molecular Formula: C14H15NO
• Molecular Weight: 213.2750
• MDL Number: MFCD00074959
• SMILES: N[C@@H]([C@H](c1ccccc1)O)c1ccccc1

Computed Properties

• Complexity: 195
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 1.3

Literature

• Synthesis of dendrimer-type chiral stationary phases based on the selector of (1S,2R)-(+)-2-amino-1,2-diphenylethanol derivate and their enantioseparation evaluation by HPLC.

  Chirality 20100101

• NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds.

  Bioorganic & medicinal chemistry 20090501

• Immobilization of (1S,2R)-(+)-2-amino-1,2-diphenylethanol derivates on aminated silica gel with different linkages as chiral stationary phases and their enantioseparation evaluation by HPLC.

  Chirality 20090401

• Asymmetric synthesis of [2,3-(13)C(2),(15)N]-4-benzyloxy-5,6-diphenyl-2,3,5,6-tetrahydro-4H-oxazine-2-one via lipase TL-mediated kinetic resolution of benzoin: general procedure for the synthesis of [2,3-(13)C(2),(15)N]-L-alanine.

  The Journal of organic chemistry 20011130

• Solid-phase synthesis of homogeneous ruthenium catalysts on silica for the continuous asymmetric transfer hydrogenation reaction.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20010316