5-(4-fluoro-3-methoxyphenyl)pyridine-3-carboxylic acid|1261934-09-1,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

5-(4-fluoro-3-methoxyphenyl)pyridine-3-carboxylic acid

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Chemical Name:	5-(4-fluoro-3-methoxyphenyl)pyridine-3-carboxylic acid
CAS Number:	1261934-09-1
Product Number:	AG000S7K(AGN-PC-09Q3R0)
Synonyms:
MDL No:
Molecular Formula:	C13H10FNO3
Molecular Weight:	247.2218

Identification/Properties
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NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

247.225g/mol

XLogP3:

2.1

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

247.064g/mol

Monoisotopic Mass:

247.064g/mol

Topological Polar Surface Area:

59.4A^2

Heavy Atom Count:

Formal Charge:

Complexity:

300

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

The compound 5-(4-Fluoro-3-methoxyphenyl)nicotinic acid, also known as $name$, is commonly employed in chemical synthesis as a key building block in the production of pharmaceuticals, agrochemicals, and functional materials. Its unique structure allows for the introduction of specific functional groups and modifications, making it a versatile intermediate in organic synthesis.$name$ is utilized in the creation of various bioactive compounds due to its ability to participate in diverse chemical reactions such as esterification, amidation, and Suzuki-Miyaura cross-coupling. This compound serves as a crucial precursor in the synthesis of potential drug candidates, including anti-inflammatory agents, antimicrobial drugs, and enzyme inhibitors.In addition to its pharmaceutical applications, $name$ is also valuable in material science for the development of polymers, dyes, and other fine chemicals. Its role in chemical synthesis extends to the creation of novel molecular structures with tailored properties for specific industrial purposes.Overall, the versatility and reactivity of 5-(4-Fluoro-3-methoxyphenyl)nicotinic acid make it an indispensable component in the toolkit of synthetic chemists, enabling the creation of diverse compounds with varied functionalities and applications in the fields of medicine, agriculture, and materials science.