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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)-

Furan, 2,5-diphenyl-

c1ccc(cc1)c1ccc(o1)c1ccccc1 Request for Quotation
Chemical Name: Furan, 2,5-diphenyl-
CAS Number: 955-83-9
Product Number: AG003G10(AGN-PC-0JL9NR)
Synonyms:
MDL No:
Molecular Formula: C16H12O
Molecular Weight: 220.2659

Identification/Properties

Properties
MP:
86-90 °C
BP:
345°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5800 (estimate)
Computed Properties
Molecular Weight:
220.271g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
220.089g/mol
Monoisotopic Mass:
220.089g/mol
Topological Polar Surface Area:
13.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
202
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Diphenylfuran plays a crucial role in chemical synthesis as a versatile building block that enables the creation of various organic compounds. Its unique structure and reactivity make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials. By serving as a starting material in different reactions such as cross-coupling, oxidation, and reduction processes, 2,5-Diphenylfuran allows chemists to access a wide range of structurally diverse molecules with potential applications in drug discovery, materials science, and more. Its ability to undergo functionalization at multiple positions makes it a valuable tool for developing new chemical entities and exploring the boundaries of organic synthesis.