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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)-

Ethanone, 2,2-dibromo-1-(3,4-dimethoxyphenyl)-

COc1cc(ccc1OC)C(=O)C(Br)Br Request for Quotation
Chemical Name: Ethanone, 2,2-dibromo-1-(3,4-dimethoxyphenyl)-
CAS Number: 63987-72-4
Product Number: AG00F6L1(AGN-PC-0JOVU9)
Synonyms:
MDL No:
Molecular Formula: C10H10Br2O3
Molecular Weight: 337.9926

Identification/Properties

Computed Properties
Molecular Weight:
337.995g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
337.898g/mol
Monoisotopic Mass:
335.9g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
221
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


2,2-Dibromo-1-(3,4-dimethoxyphenyl)ethanone, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. As a powerful building block in organic chemistry, $name$ plays a crucial role in various reactions to create complex molecules with specific structures and properties.One of the key applications of 2,2-Dibromo-1-(3,4-dimethoxyphenyl)ethanone is its use in the synthesis of pharmaceutical compounds. Its unique chemical properties make it an essential intermediate in the production of novel drug molecules with potential therapeutic effects. By incorporating $name$ into the synthesis process, chemists can efficiently introduce functional groups and stereochemistry required for drug development.Furthermore, 2,2-Dibromo-1-(3,4-dimethoxyphenyl)ethanone is utilized in the preparation of advanced materials such as polymers, liquid crystals, and fine chemicals. Its ability to undergo various chemical transformations makes it a valuable tool for creating tailored materials with specific properties, including optical, electrical, or mechanical characteristics.In summary, the application of 2,2-Dibromo-1-(3,4-dimethoxyphenyl)ethanone in chemical synthesis extends beyond its simple structure, offering a wide range of possibilities for the creation of diverse molecules essential for pharmaceuticals, materials science, and other industries.