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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)-

Benzeneacetic acid, 2-fluoro-4-hydroxy-, methyl ester

COC(=O)Cc1ccc(cc1F)O Request for Quotation
Chemical Name: Benzeneacetic acid, 2-fluoro-4-hydroxy-, methyl ester
CAS Number: 91361-59-0
Product Number: AG00H4V9(AGN-PC-0CDVKH)
Synonyms:
MDL No:
Molecular Formula: C9H9FO3
Molecular Weight: 184.1644

Identification/Properties

Computed Properties
Molecular Weight:
184.166g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
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:
184
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:
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


Methyl 2-(2-fluoro-4-hydroxyphenyl)acetate, often used as a versatile building block in chemical synthesis due to its unique chemical properties. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and flavors. Its structural characteristics make it a valuable component in the creation of complex molecules with specific biological activities. In organic synthesis, Methyl 2-(2-fluoro-4-hydroxyphenyl)acetate is frequently employed in the modification of natural products, the development of new drug candidates, and the synthesis of functional materials. Its presence can enhance the potency and specificity of bioactive compounds, contributing to advancements in the fields of medicine and materials science.