Home Other Building Blocks (1S,2R)-(+)-2-Amino-1,2-diphenylethanol

(1S,2R)-(+)-2-Amino-1,2-diphenylethanol

CAS No.:
23364-44-5
Catalog Number:
AG002MZX
Molecular Formula:
C14H15NO
Molecular Weight:
213.2750
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$32
- +
25g
98%
In Stock USA
United States
$67
- +
100g
98%
In Stock USA
United States
$250
- +
Product Description
Catalog Number:
AG002MZX
Chemical Name:
(1S,2R)-(+)-2-Amino-1,2-diphenylethanol
CAS Number:
23364-44-5
Molecular Formula:
C14H15NO
Molecular Weight:
213.2750
MDL Number:
MFCD00074959
IUPAC Name:
(1S,2R)-2-amino-1,2-diphenylethanol
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+/m1/s1
InChI Key:
GEJJWYZZKKKSEV-KGLIPLIRSA-N
SMILES:
N[C@@H]([C@H](c1ccccc1)O)c1ccccc1
Properties
Complexity:
195  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
213.115g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
213.28g/mol
Monoisotopic Mass:
213.115g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
46.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3  
Literature
Title Journal
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
Properties