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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, 1,1,2,2-tetraphenyl-

OC(C(c1ccccc1)(c1ccccc1)O)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 1,2-Ethanediol, 1,1,2,2-tetraphenyl-
CAS Number: 464-72-2
Product Number: AG003O2P(AGN-PC-0JM0V2)
Synonyms:
MDL No:
Molecular Formula: C26H22O2
Molecular Weight: 366.4517

Identification/Properties

Properties
MP:
171-173 °C(lit.)
BP:
506.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.4875 (estimate)
Computed Properties
Molecular Weight:
366.46g/mol
XLogP3:
4.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
366.162g/mol
Monoisotopic Mass:
366.162g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
383
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tetraphenylethylene Glycol, a versatile compound widely employed in chemical synthesis, serves as a valuable building block in organic chemistry. Its unique chemical structure, characterized by multiple phenyl rings and a glycol moiety, offers a range of applications in the synthesis of complex molecules and functional materials.In the realm of organic synthesis, Tetraphenylethylene Glycol plays a crucial role as a bridging unit for constructing elaborate molecular frameworks. By utilizing its phenyl groups as reactive sites for various functionalization reactions, chemists can tailor its properties to meet specific requirements in designing novel compounds. Furthermore, the presence of the glycol moiety introduces flexibility and solubility enhancements, expanding its utility in diverse synthetic approaches.The incorporation of Tetraphenylethylene Glycol in the synthesis of supramolecular architectures and advanced materials underscores its significance in driving innovation within the chemical industry. Its ability to participate in non-covalent interactions, such as π-π stacking and hydrogen bonding, facilitates the assembly of intricate structures with tailored properties and functionalities. This capability holds promise for applications ranging from optoelectronic devices to drug delivery systems, where precise control over molecular organization is paramount.Overall, Tetraphenylethylene Glycol stands out as a versatile synthetic building block with immense potential for advancing chemical research and development. Its unique structural features and versatile reactivity pave the way for the creation of new molecules and materials with tailored properties, making it a valuable asset in the toolbox of synthetic chemists seeking to push the boundaries of molecular design and innovation.