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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)-

2-fluoro-5-methoxy-4-methylbenzoic acid

COc1cc(C(=O)O)c(cc1C)F Request for Quotation
Chemical Name: 2-fluoro-5-methoxy-4-methylbenzoic acid
CAS Number: 870221-15-1
Product Number: AG00GZPI(AGN-PC-0H7VXJ)
Synonyms:
MDL No:
Molecular Formula: C9H9FO3
Molecular Weight: 184.1644

Identification/Properties

Computed Properties
Molecular Weight:
184.166g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
184.054g/mol
Monoisotopic Mass:
184.054g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
195
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-Fluoro-5-methoxy-4-methylbenzoic acid, also known as $name$, serves as a versatile building block in chemical synthesis. With its unique structure, this compound plays a crucial role in the development of various organic compounds and pharmaceuticals. Its fluorine and methoxy functional groups provide opportunities for selective reactions and modifications, making it a valuable tool in the synthesis of complex molecules.2-Fluoro-5-methoxy-4-methylbenzoic acid can be utilized as a key intermediate in the production of agrochemicals, pharmaceuticals, and materials science. Its presence in a synthetic pathway can enable the introduction of specific functional groups or stereochemistry, leading to the creation of new compounds with enhanced properties. Additionally, this compound can serve as a precursor for the synthesis of biologically active molecules, such as antimicrobial agents or enzyme inhibitors.Furthermore, the reactivity of 2-Fluoro-5-methoxy-4-methylbenzoic acid allows for efficient transformations into various derivatives, expanding its applications in organic synthesis. By incorporating this compound into chemical reactions, researchers can access a diverse array of molecular structures with tailored features and functionalities. Overall, the strategic incorporation of 2-Fluoro-5-methoxy-4-methylbenzoic acid in chemical synthesis offers a promising avenue for the exploration and development of novel compounds with potential applications across different industries.