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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)-

Benzenepropanoic acid, 2-chloro-4-fluoro-

OC(=O)CCc1ccc(cc1Cl)F Request for Quotation
Chemical Name: Benzenepropanoic acid, 2-chloro-4-fluoro-
CAS Number: 174603-38-4
Product Number: AG001ZST(AGN-PC-00FSPG)
Synonyms:
MDL No: MFCD06656905
Molecular Formula: C9H8ClFO2
Molecular Weight: 202.6100

Identification/Properties

Computed Properties
Molecular Weight:
202.609g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
202.02g/mol
Monoisotopic Mass:
202.02g/mol
Topological Polar Surface Area:
37.3A^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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(2-Chloro-4-fluorophenyl)propanoic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in organic chemistry as a key intermediate in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. With its unique structure, $name$ serves as a valuable building block for the synthesis of more complex molecules through various chemical reactions.In chemical synthesis, 3-(2-Chloro-4-fluorophenyl)propanoic acid can be used as a precursor in the preparation of diverse compounds with both medicinal and industrial applications. Its functional groups make it a convenient starting material for the introduction of additional substituents or modifications, allowing for the creation of structurally diverse molecules. By employing different synthetic strategies, chemists can incorporate this compound into the synthesis of drugs, pesticides, fragrances, and other specialized chemicals.Moreover, the versatility of 3-(2-Chloro-4-fluorophenyl)propanoic acid enables researchers to explore innovative synthetic routes and develop new compounds with enhanced properties. Its presence in the chemical synthesis toolbox facilitates the efficient production of valuable compounds with targeted biological activities or desired characteristics. Overall, the application of $name$ in chemical synthesis showcases its significance as a fundamental building block for creating complex molecules with diverse functionalities.