23190-16-1 | (1R,2S)-(-)-2-Amino-1,2-diphenylethanol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$9.00	$6.00
10g	98%	in stock	$15.00	$10.00
25g	98%	in stock	$28.00	$19.00
100g	98%	in stock	$93.00	$65.00

Description

• Catalog Number: AB54646
• Chemical Name: (1R,2S)-(-)-2-Amino-1,2-diphenylethanol
• CAS Number: 23190-16-1
• Molecular Formula: C14H15NO
• Molecular Weight: 213.275
• MDL Number: MFCD00074960
• 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

• Beta-amino alcohol derived beta-hydroxy- and beta-(o-diphenylphosphino)benzoyloxy(o-diphenylphosphino)benzamides: an ester-amide ligand structural model for the palladium-catalyzed allylic alkylation reaction.

  The Journal of organic chemistry 20091106

• 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

• A solid-state fluorescent host system with a 2(1)-helical column consisting of chiral (1R,2S)-2-amino-1,2-diphenylethanol and fluorescent 1-pyrenecarboxylic acid.

  Chemistry, an Asian journal 20080307

• A solid-state fluorescence sensing system consisting of chiral (1R,2S)-2-amino-1,2-diphenylethanol and fluorescent 2-anthracenecarboxylic acid.

  Organic letters 20070816

• Synthesis of C3-symmetric tris(beta-hydroxy amide) ligands and their Ti(IV) complex-catalyzed enantioselective alkynylation of aldehydes.

  Organic letters 20050526

• Efficient crystallization-induced dynamic resolution of alpha-substituted carboxylic acids.

  The Journal of organic chemistry 20040611

• Modification of (1R,2S)-1,2-diphenyl-2-aminoethanol for the highly enantioselective, asymmetric alkylation of N-diphenylphosphinoyl arylimines with dialkylzinc.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20040319

• An amino alcohol ligand for highly enantioselective addition of organozinc reagents to aldehydes: serendipity rules.

  Organic letters 20020627

• 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