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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)-

1,8-Anthracenedicarboxylic acid, dimethyl ester

COC(=O)c1cccc2c1cc1c(c2)cccc1C(=O)OC Request for Quotation
Chemical Name: 1,8-Anthracenedicarboxylic acid, dimethyl ester
CAS Number: 93655-34-6
Product Number: AG003PKS(AGN-PC-0LPA55)
Synonyms:
MDL No:
Molecular Formula: C18H14O4
Molecular Weight: 294.30136

Identification/Properties

Properties
MP:
105℃
Form:
Solid
Computed Properties
Molecular Weight:
294.306g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
294.089g/mol
Monoisotopic Mass:
294.089g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
395
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Dimethyl Anthracene-1,8-dicarboxylate is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound serves as a crucial building block in the creation of various organic molecules with significant applications in pharmaceuticals, materials science, and the development of specialty chemicals. In chemical synthesis, Dimethyl Anthracene-1,8-dicarboxylate acts as a key intermediate for generating complex molecular structures through various reactions such as esterifications, carbon-carbon bond formations, and cycloadditions. Its particular molecular architecture allows for precise manipulation and modification, enabling chemists to tailor the properties and functionalities of the final products. Moreover, Dimethyl Anthracene-1,8-dicarboxylate's presence brings about distinct characteristics to the synthesized compounds, imparting beneficial properties such as enhanced stability, reactivity, and selectivity. Its inclusion in organic reactions facilitates the synthesis of compounds with specific chirality, functional groups, or geometries, contributing to the advancement of diverse fields within the chemical industry.Overall, the strategic utilization of Dimethyl Anthracene-1,8-dicarboxylate in chemical synthesis enables researchers to access a wide range of novel molecules and materials with tailored properties, paving the way for innovative advancements in various applications.