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

Name: (1R,2S)-2-Amino-1,2-diphenylethanol
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB017972
Product Name:	(1R,2S)-2-Amino-1,2-diphenylethanol
CAS:	23190-16-1
Synonyms:	(1R,2S)-2-amino-1,2-diphenylethanol; (1R,2S)-2-amino-1,2-diphenylethanol
Application:	(1R,2S)-(−)-2-Amino-1,2-diphenylethanol is a chiral auxilliary useful for synthesis and coupling reactions

Technical Data

IUPAC Name:	(1R,2S)-2-amino-1,2-diphenylethanol
Description:	(1R,2S)-(-)-2-Amino-1,2-diphenylethanol (CAS# 23190-16-1) is a chiral auxilliary useful for synthesis and coupling reactions.
Molecular Weight:	213.28
Molecular Formula:	C14H15NO
Canonical SMILES:	C1=CC=C(C=C1)C(C(C2=CC=CC=C2)O)N
InChI:	InChI=1S/C14H15NO/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-14,16H,15H2/t13-,14+/m0/s1
InChI Key:	GEJJWYZZKKKSEV-UONOGXRCSA-N
Boiling Point:	374.3 °C at 760 mmHg
Melting Point:	142-144 °C
Purity:	≥ 98 %, ≥ 95 % e.e.
Density:	1.148 g/cm³
Appearance:	White or off-white crystalline powder
Storage:	Room temperature.
MDL:	MFCD00074960
LogP:	3.12030

GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

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PMID	Publication Date	Title	Journal
19319988	20100101	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
19807143	20091106	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
19345586	20090501	NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds	Bioorganic & medicinal chemistry
18655165	20090401	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
18293291	20080307	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

Complexity:	195
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	2
Defined Bond Stereocenter Count:	0
Exact Mass:	213.115364102
Formal Charge:	0
Heavy Atom Count:	16
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	213.115364102
Rotatable Bond Count:	3
Topological Polar Surface Area:	46.2 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.3