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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,2-Ethanediol, 1,1,2-triphenyl-, (2R)-

O[C@@H](C(c1ccccc1)(c1ccccc1)O)c1ccccc1 Request for Quotation
Chemical Name: 1,2-Ethanediol, 1,1,2-triphenyl-, (2R)-
CAS Number: 95061-46-4
Product Number: AG0066IO(AGN-PC-0OO0LJ)
Synonyms:
MDL No: MFCD00134424
Molecular Formula: C20H18O2
Molecular Weight: 290.3557

Identification/Properties

Properties
MP:
126 °C
BP:
452.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
220 ° (C=1, EtOH)
Computed Properties
Molecular Weight:
290.362g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
290.131g/mol
Monoisotopic Mass:
290.131g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
305
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-1,1,2-Triphenyl-1,2-ethanediol is a versatile compound widely employed in chemical synthesis due to its unique structural properties. This compound serves as a key building block in various organic reactions, especially in the field of asymmetric synthesis. Its chiral nature makes it particularly valuable in the creation of enantiomerically enriched products. Additionally, (R)-1,1,2-Triphenyl-1,2-ethanediol can act as a ligand in transition metal-catalyzed reactions, enhancing the selectivity and efficiency of the synthesis process. Its application extends to the preparation of pharmaceutical intermediates, natural product synthesis, and material science research.