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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)-

ETHYL 2-FLUORO-4-(METHYLSULFONYL)BENZOATE

CCOC(=O)c1ccc(cc1F)S(=O)(=O)C Request for Quotation
Chemical Name: ETHYL 2-FLUORO-4-(METHYLSULFONYL)BENZOATE
CAS Number: 1354940-65-0
Product Number: AG003Q42(AGN-PC-0WAM4S)
Synonyms:
MDL No: MFCD21332899
Molecular Formula: C10H11FO4S
Molecular Weight: 246.2553

Identification/Properties

Properties
Storage:
Room Temperature;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-fluoro-4-(methylsulfonyl)benzoate is a versatile compound used in chemical synthesis due to its unique properties and reactivity. This compound serves as an important building block in the development of various pharmaceuticals, agrochemicals, and materials.In organic synthesis, Ethyl 2-fluoro-4-(methylsulfonyl)benzoate can participate in a range of reactions to introduce the fluorine and methylsulfonyl functional groups into target molecules. The fluoro substituent can serve as a key structural element, influencing the compound's biological activity or physicochemical properties. The methylsulfonyl group, on the other hand, can act as a protecting group or a functional group for further transformations.Furthermore, the ester functionality of Ethyl 2-fluoro-4-(methylsulfonyl)benzoate provides opportunities for derivatization through esterification or transesterification reactions. This enables chemists to modify the compound's solubility, stability, or interactions with biological targets.Overall, Ethyl 2-fluoro-4-(methylsulfonyl)benzoate is a valuable component in the toolkit of synthetic chemists, allowing for the efficient construction of complex molecules with tailored properties for a range of applications.