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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-(5-fluoro-2-methoxyphenyl)-

COc1ccc(cc1C(=O)CBr)F Request for Quotation
Chemical Name: Ethanone, 2-bromo-1-(5-fluoro-2-methoxyphenyl)-
CAS Number: 343-04-4
Product Number: AG0038SW(AGN-PC-0KKLFN)
Synonyms:
MDL No:
Molecular Formula: C9H8BrFO2
Molecular Weight: 247.0610

Identification/Properties

Computed Properties
Molecular Weight:
247.063g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
245.969g/mol
Monoisotopic Mass:
245.969g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
187
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-(5-fluoro-2-methoxyphenyl)ethanone is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in organic chemistry, playing a crucial role in various reactions and pathways.One of the primary applications of 2-Bromo-1-(5-fluoro-2-methoxyphenyl)ethanone is in the synthesis of complex organic molecules, particularly pharmaceutical intermediates. Its functional groups enable it to participate in a range of important transformations, such as nucleophilic substitution reactions and cross-coupling reactions.Furthermore, this compound can be used to introduce specific structural motifs into target molecules, enhancing their biological activity or physical properties. Its ability to selectively react with different reagents makes it a valuable tool for chemists seeking to design and synthesize novel compounds with tailored characteristics.Overall, 2-Bromo-1-(5-fluoro-2-methoxyphenyl)ethanone is a crucial component in the toolkit of synthetic chemists, facilitating the preparation of diverse molecules with potential applications in drug discovery, materials science, and other fields. Its versatility and reactivity make it a valuable asset in the realm of chemical synthesis.