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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)-

Phenol, 4,4'-(1-methylethylidene)bis-, diacetate

CC(=O)Oc1ccc(cc1)C(c1ccc(cc1)OC(=O)C)(C)C Request for Quotation
Chemical Name: Phenol, 4,4'-(1-methylethylidene)bis-, diacetate
CAS Number: 10192-62-8
Product Number: AG0005YO(AGN-PC-0IVTIG)
Synonyms:
MDL No:
Molecular Formula: C19H20O4
Molecular Weight: 312.3597

Identification/Properties

Properties
MP:
91-94℃ (lit.)
Form:
Solid
Computed Properties
Molecular Weight:
312.365g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
312.136g/mol
Monoisotopic Mass:
312.136g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
375
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


The application of Propane-2,2-diylbis(4,1-phenylene) diacetate in chemical synthesis lies in its role as a versatile reagent and building block in organic reactions. This compound, known for its bifunctional nature, serves as an important intermediate in the synthesis of various complex organic molecules. It enables the formation of intricate chemical structures through its ability to undergo multiple functional group transformations. In further chemical reactions, Propane-2,2-diylbis(4,1-phenylene) diacetate can participate in cross-coupling reactions, cycloadditions, and other key processes, leading to the creation of novel compounds with diverse applications in pharmaceuticals, materials science, and other fields. By incorporating Propane-2,2-diylbis(4,1-phenylene) diacetate into synthetic pathways, chemists can access unique structural motifs, enhancing the development of new molecules with tailored properties and functionalities.