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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)-

Benzoic acid, 2-fluoro-3,5-dimethoxy-, methyl ester

COc1cc(OC)c(c(c1)C(=O)OC)F Request for Quotation
Chemical Name: Benzoic acid, 2-fluoro-3,5-dimethoxy-, methyl ester
CAS Number: 651734-58-6
Product Number: AG00EKFA(AGN-PC-0CYCE9)
Synonyms:
MDL No:
Molecular Formula: C10H11FO4
Molecular Weight: 214.1903

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
214.192g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
214.064g/mol
Monoisotopic Mass:
214.064g/mol
Topological Polar Surface Area:
44.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
222
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-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-fluoro-3,5-dimethoxybenzoate is a compound commonly used in chemical synthesis as a versatile building block for the creation of various organic molecules. Specifically, it serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties.In chemical synthesis, Methyl 2-fluoro-3,5-dimethoxybenzoate can undergo a range of transformations, such as nucleophilic substitution, oxidation, and reduction reactions, to generate structurally diverse compounds with tailored functionalities. Its fluorine atom offers opportunities for introducing fluorinated motifs into target molecules, which can enhance their biological activity or chemical properties.Furthermore, the dimethoxybenzoate moiety provides a site for further derivatization, enabling the attachment of different functional groups to modulate the compound's solubility, stability, and reactivity. This makes Methyl 2-fluoro-3,5-dimethoxybenzoate a valuable tool in the synthesis of complex organic molecules with potential applications in drug discovery, materials science, and other fields requiring precise chemical manipulation.