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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)-

[1,1'-Biphenyl]-2,2'-diol, 3,3'-dimethoxy-5,5'-dimethyl-

COc1cc(C)cc(c1O)c1cc(C)cc(c1O)OC Request for Quotation
Chemical Name: [1,1'-Biphenyl]-2,2'-diol, 3,3'-dimethoxy-5,5'-dimethyl-
CAS Number: 13990-86-8
Product Number: AG001BS9(AGN-PC-0JPPMA)
Synonyms:
MDL No:
Molecular Formula: C16H18O4
Molecular Weight: 274.3117

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
274.316g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
274.121g/mol
Monoisotopic Mass:
274.121g/mol
Topological Polar Surface Area:
58.9A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
279
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


3,3'-Dimethoxy-5,5'-dimethylbiphenyl-2,2'-diol, commonly known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in organic chemistry as a key building block for the synthesis of various molecular structures.In chemical synthesis, $name$ is frequently utilized as a precursor in the preparation of complex organic compounds. Its unique structure and reactivity make it a valuable starting material for the synthesis of novel pharmaceuticals, agrochemicals, and materials with tailored properties.One of the primary applications of $name$ in chemical synthesis is in the preparation of biaryl compounds. By utilizing $name$ as a starting material, chemists can efficiently access diverse biaryl structures through cross-coupling reactions, such as Suzuki-Miyaura coupling and Buchwald-Hartwig amination. These biaryl compounds are essential components in the development of pharmaceuticals, natural product synthesis, and materials science.Furthermore, $name$ also serves as a valuable intermediate in the synthesis of liquid crystals, dyes, and organic electronic materials. Its structural flexibility and functional groups allow for the introduction of various substituents and modifications, enabling the tailored design of organic molecules for specific applications.Overall, the use of 3,3'-Dimethoxy-5,5'-dimethylbiphenyl-2,2'-diol in chemical synthesis underscores its importance as a versatile building block for the creation of diverse organic compounds with high synthetic and structural utility.