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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)-

6-bromo-2-fluoro-3-methoxybenzoic acid

COc1ccc(c(c1F)C(=O)O)Br Request for Quotation
Chemical Name: 6-bromo-2-fluoro-3-methoxybenzoic acid
CAS Number: 935534-45-5
Product Number: AG00IHNX(AGN-PC-09TAH4)
Synonyms:
MDL No:
Molecular Formula: C8H6BrFO3
Molecular Weight: 249.0338

Identification/Properties

Computed Properties
Molecular Weight:
249.035g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
247.948g/mol
Monoisotopic Mass:
247.948g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
200
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


6-Bromo-2-fluoro-3-methoxybenzoic acid, also known as $name$, is a valuable compound widely used in chemical synthesis due to its unique properties and versatile applications. In organic chemistry, this compound serves as a key building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its strategic positioning of bromine, fluorine, and methoxy functional groups on the benzene ring makes it a valuable intermediate in the synthesis of complex molecules. Through appropriate functional group transformations, $name$ can be utilized for the generation of diverse chemical structures with tailored properties and activities. Its compatibility with a wide range of reaction conditions and ability to undergo selective modifications make it a versatile tool for synthetic chemists seeking to access novel compounds for research and development purposes.