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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)-

Oxirane, 2,3-diphenyl-, (2R,3R)-rel-

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Chemical Name: Oxirane, 2,3-diphenyl-, (2R,3R)-rel-
CAS Number: 1439-07-2
Product Number: AG003UZC(AGN-PC-0PUQZX)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
65-67 °C(lit.)
BP:
273.14°C (rough estimate)
Storage:
2-8℃;
Form:
Solid
Refractive Index:
1.4700 (estimate)
Computed Properties
Molecular Weight:
196.249g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
196.089g/mol
Monoisotopic Mass:
196.089g/mol
Topological Polar Surface Area:
12.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
179
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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#:
-
Hazard Statements:
H302+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P363-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Trans-1,2-Diphenylethylene oxide, also known as styrene oxide, is a versatile compound widely used in chemical synthesis for various applications. In organic chemistry, it serves as a key building block in the synthesis of complex organic molecules, due to its ability to undergo nucleophilic ring-opening reactions. One of its important applications is as a precursor in the synthesis of chiral epoxides, which are essential intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, trans-1,2-Diphenylethylene oxide can be used as a reagent in the preparation of epoxy resins, which find extensive use in coatings, adhesives, and composites industries. Its unique chemical properties and reactivity make it a valuable tool for chemists in the design and synthesis of novel compounds with diverse functionalities.