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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)-

4-Fluoro-2-(1-pyrrolidinyl)benzoic Acid

OC(=O)c1ccc(cc1N1CCCC1)F Request for Quotation
Chemical Name: 4-Fluoro-2-(1-pyrrolidinyl)benzoic Acid
CAS Number: 952680-24-9
Product Number: AG003LCU(AGN-PC-0WAFRY)
Synonyms:
MDL No:
Molecular Formula: C11H12FNO2
Molecular Weight: 209.2169

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
209.22g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
209.085g/mol
Monoisotopic Mass:
209.085g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
241
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:
Danger
UN#:
2811
Hazard Statements:
H301-H311-H331
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Fluoro-2-(1-pyrrolidinyl)benzoic Acid is a versatile compound widely used in chemical synthesis as a key building block for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a crucial intermediate in the synthesis of complex organic molecules with important biological activities. Specifically, its unique structural features make it a valuable precursor for the creation of novel drug candidates, agricultural products, and functional materials. By incorporating this compound into synthetic routes, chemists can access a diverse range of target compounds with tailored properties and enhanced activities. Furthermore, the presence of the fluoro and pyrrolidinyl functionalities in this molecule imparts specific reactivity and selectivity in various chemical transformations, allowing for efficient and controlled synthesis of desired products in the laboratory or industrial settings.