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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)-

2-(2-fluorophenyl)-1,3-thiazole-4-carboxylic acid

Fc1ccccc1c1scc(n1)C(=O)O Request for Quotation
Chemical Name: 2-(2-fluorophenyl)-1,3-thiazole-4-carboxylic acid
CAS Number: 1094373-86-0
Product Number: AG00924O(AGN-PC-06GK7F)
Synonyms:
MDL No:
Molecular Formula: C10H6FNO2S
Molecular Weight: 223.2235

Identification/Properties

Computed Properties
Molecular Weight:
223.221g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
223.01g/mol
Monoisotopic Mass:
223.01g/mol
Topological Polar Surface Area:
78.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
252
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-Fluorophenyl)thiazole-4-carboxylic acid is a key intermediate in organic synthesis with diverse applications in chemical research and development. Known for its unique structure and reactivity, this compound serves as a versatile building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-(2-Fluorophenyl)thiazole-4-carboxylic acid is commonly used as a precursor for the creation of complex molecules. Its functional groups and molecular scaffold enable the introduction of additional substituents or modifications to tailor the properties of the final product. This acid can participate in numerous organic reactions such as esterification, amidation, oxidation, and reduction, allowing for the strategic construction of intricate molecular structures.Furthermore, the incorporation of 2-(2-Fluorophenyl)thiazole-4-carboxylic acid into synthetic pathways can impart specific properties to the target compounds. The thiazole ring confers aromaticity and potential for π-π interactions, while the carboxylic acid group offers versatility for further derivatization or manipulation. These characteristics make this compound valuable in medicinal chemistry for designing bioactive molecules with desired pharmacological profiles.Overall, the strategic utilization of 2-(2-Fluorophenyl)thiazole-4-carboxylic acid in chemical synthesis enables the efficient construction of structurally complex and functionally diverse molecules, making it a valuable tool for researchers and synthetic chemists alike.