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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)-

Cyclopentanecarboxylic acid, 1-(3-fluorophenyl)-

Fc1cccc(c1)C1(CCCC1)C(=O)O Request for Quotation
Chemical Name: Cyclopentanecarboxylic acid, 1-(3-fluorophenyl)-
CAS Number: 214262-97-2
Product Number: AG007QK8(AGN-PC-0JVO85)
Synonyms:
MDL No:
Molecular Formula: C12H13FO2
Molecular Weight: 208.2288

Identification/Properties

Computed Properties
Molecular Weight:
208.232g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
208.09g/mol
Monoisotopic Mass:
208.09g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
246
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-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 1-(3-Fluorophenyl)cyclopentanecarboxylic acid is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the primary applications of 1-(3-Fluorophenyl)cyclopentanecarboxylic acid is its role as a precursor in the production of cyclopentanone derivatives. These derivatives are essential intermediates in the synthesis of complex organic compounds, including biologically active molecules and natural products. The presence of the fluorine substituent on the phenyl ring of the compound enhances the reactivity and specificity of the reactions, allowing for efficient and selective transformations in chemical synthesis.Furthermore, the cyclopentanecarboxylic acid moiety in this compound provides a versatile platform for further functionalization through various synthetic methods, such as esterification, amidation, and decarboxylation. This allows for the introduction of different functional groups to tailor the properties of the final products for specific applications in medicinal chemistry, material science, and other fields.Overall, the 1-(3-Fluorophenyl)cyclopentanecarboxylic acid is a valuable tool in the hands of synthetic chemists, enabling the synthesis of diverse and complex molecules with potential applications in pharmaceuticals, agriculture, and other industries.