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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)-

Propanoic acid, 3-(2-fluorophenoxy)-

OC(=O)CCOc1ccccc1F Request for Quotation
Chemical Name: Propanoic acid, 3-(2-fluorophenoxy)-
CAS Number: 2967-72-8
Product Number: AG002Z1L(AGN-PC-0K6MQV)
Synonyms:
MDL No:
Molecular Formula: C9H9FO3
Molecular Weight: 184.1644

Identification/Properties

Properties
BP:
282.5 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
184.166g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
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:
172
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-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The use of 3-(2-Fluorophenoxy)propanoic acid in chemical synthesis is particularly valuable for its versatility and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. By leveraging the unique structural features of 3-(2-Fluorophenoxy)propanoic acid, chemists are able to introduce specific functional groups and manipulate its properties through further derivatization. This enables the synthesis of a wide range of novel compounds with tailored characteristics and applications in diverse fields such as medicine, agriculture, and materials science. As a result, 3-(2-Fluorophenoxy)propanoic acid plays a crucial role in advancing the frontier of chemical research and innovation.