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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-bromo-1-(2,5-dimethoxyphenyl)-

COc1ccc(c(c1)C(=O)CBr)OC Request for Quotation
Chemical Name: Ethanone, 2-bromo-1-(2,5-dimethoxyphenyl)-
CAS Number: 1204-21-3
Product Number: AG003B6A(AGN-PC-0JLA2H)
Synonyms:
MDL No:
Molecular Formula: C10H11BrO3
Molecular Weight: 259.0965

Identification/Properties

Properties
MP:
83-85 °C(lit.)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
1.4620 (estimate)
Computed Properties
Molecular Weight:
259.099g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
257.989g/mol
Monoisotopic Mass:
257.989g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
196
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:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-1-(2,5-dimethoxyphenyl)ethanone, also known as DBMC, is commonly used in chemical synthesis as a versatile building block for creating various organic compounds. Its unique structure incorporates a bromine atom and a 2,5-dimethoxyphenyl group, making it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, 2-Bromo-1-(2,5-dimethoxyphenyl)ethanone serves as a key reagent for introducing functional groups such as the bromine atom and the phenyl ring into target molecules. It can undergo various organic reactions, including nucleophilic substitution, acylation, and Grignard reactions, to form complex organic structures with high regioselectivity and yield.Additionally, this compound is widely utilized in the synthesis of natural products, heterocyclic compounds, and biologically active molecules due to its ability to selectively modify specific positions on aromatic rings and carbonyl groups. Its versatility and reactivity make it a valuable tool for chemists and researchers seeking to develop new compounds with tailored properties and functions.