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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)-

Methanone, (3,4-dihydroxyphenyl)(2,4,6-trihydroxyphenyl)-

Oc1cc(O)c(c(c1)O)C(=O)c1ccc(c(c1)O)O Request for Quotation
Chemical Name: Methanone, (3,4-dihydroxyphenyl)(2,4,6-trihydroxyphenyl)-
CAS Number: 519-34-6
Product Number: AG00DDWC(AGN-PC-0JL8BU)
Synonyms:
MDL No:
Molecular Formula: C13H10O6
Molecular Weight: 262.2149

Identification/Properties

Computed Properties
Molecular Weight:
262.217g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
262.048g/mol
Monoisotopic Mass:
262.048g/mol
Topological Polar Surface Area:
118A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
321
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:
Danger
UN#:
3077
Hazard Statements:
H319-H400
Precautionary Statements:
P273-P305+P351+P338
Class:
9
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Maclurin, also known as Maclurin derived from Maclura pomifera, is a type of natural phenolic compound that has found diverse applications in chemical synthesis. In organic chemistry, Maclurin is often utilized as a starting material or reagent in various reactions due to its unique chemical properties. One of its primary applications is as a precursor for the synthesis of diversified bioactive compounds. Maclurin serves as a valuable building block in the development of new pharmaceuticals, agrochemicals, and materials. Its structural versatility allows for modification through chemical reactions, enabling the creation of structurally complex molecules. Furthermore, Maclurin has demonstrated potential in the synthesis of natural product analogs and functionalized derivatives with enhanced properties. Researchers continue to explore the full potential of Maclurin in chemical synthesis for the development of innovative compounds with applications across multiple disciplines within the field of chemistry.