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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)-

9(10H)-Anthracenone, 10,10-dimethyl-

O=C1c2ccccc2C(c2c1cccc2)(C)C Request for Quotation
Chemical Name: 9(10H)-Anthracenone, 10,10-dimethyl-
CAS Number: 5447-86-9
Product Number: AG0032NQ(AGN-PC-07Y4JA)
Synonyms:
MDL No:
Molecular Formula: C16H14O
Molecular Weight: 222.2818

Identification/Properties

Properties
MP:
101-103°C
BP:
346.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
222.287g/mol
XLogP3:
4.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
222.104g/mol
Monoisotopic Mass:
222.104g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
290
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

PNMR/1010-DIMETHYL-910-DIHYDROANTHRACEN-9-ONE-5447-86-9-hnmr.pdf

Other Analytical Data

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Chemical Structure


10,10-Dimethylanthrone is a versatile compound commonly used in chemical synthesis as a key building block for various applications. In organic chemistry, it serves as a valuable precursor in the synthesis of heterocyclic compounds and complex organic molecules. Its unique structure and reactivity make it an important intermediate in the production of pharmaceuticals, agrochemicals, and materials science. With its strong electron-withdrawing carbonyl group, 10,10-Dimethylanthrone undergoes a range of reactions including alkylation, acylation, and condensation, enabling the creation of novel chemical structures with tailored properties. Additionally, its aromatic nature allows for effective incorporation into a variety of functional materials and polymers, contributing to the development of advanced materials with enhanced properties. In summary, 10,10-Dimethylanthrone plays a vital role in the synthesis of diverse compounds, making it a crucial tool for researchers and chemists in various fields of study.