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2325-10-2

2325-10-2 | 1,2-Ethanediol, 1,2-diphenyl-, (1S,2S)-

CAS No: 2325-10-2 Catalog No: AG002MOH MDL No:MFCD00064255

Product Description

Catalog Number:
AG002MOH
Chemical Name:
1,2-Ethanediol, 1,2-diphenyl-, (1S,2S)-
CAS Number:
2325-10-2
Molecular Formula:
C14H14O2
Molecular Weight:
214.2598
MDL Number:
MFCD00064255
IUPAC Name:
(1S,2S)-1,2-diphenylethane-1,2-diol
InChI:
InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H/t13-,14-/m0/s1
InChI Key:
IHPDTPWNFBQHEB-KBPBESRZSA-N
SMILES:
O[C@H]([C@H](c1ccccc1)O)c1ccccc1
UNII:
WX45Q7714B

Properties

Complexity:
171  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
214.099g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
214.264g/mol
Monoisotopic Mass:
214.099g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.6  

Literature

Title Journal
Determination of stability constants of complexes of neutral analytes with charged cyclodextrins by affinity capillary electrophoresis. Electrophoresis 20120301
Synthesis of (+)-polyoxamic acid and D-sorbitol from simple achiral allylic halides employing (S,S)-hydrobenzoin as a chiral source. Chemical communications (Cambridge, England) 20020521
Chiral separation of enantiomeric 1,2-diamines using molecular imprinting method and selectivity enhancement by addition of achiral primary amines into eluents. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20020101

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