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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)-

1-(3-fluorophenyl)pyrazole-4-carbaldehyde

O=Cc1cnn(c1)c1cccc(c1)F Request for Quotation
Chemical Name: 1-(3-fluorophenyl)pyrazole-4-carbaldehyde
CAS Number: 936940-82-8
Product Number: AG0061I2(AGN-PC-05W5WJ)
Synonyms:
MDL No:
Molecular Formula: C10H7FN2O
Molecular Weight: 190.1738

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
190.177g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
190.054g/mol
Monoisotopic Mass:
190.054g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
212
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


1-(3-Fluorophenyl)-1H-pyrazole-4-carbaldehyde is a versatile compound commonly used in chemical synthesis due to its reactivity and unique structural properties. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 1-(3-Fluorophenyl)-1H-pyrazole-4-carbaldehyde can act as a key intermediate in the production of heterocyclic compounds. Its functional group allows for easy modification, enabling the introduction of different substituents to tailor the properties of the final product. This compound is particularly useful in the synthesis of bioactive molecules, as its pyrazole ring structure is commonly found in many pharmaceutical compounds with diverse biological activities.Additionally, 1-(3-Fluorophenyl)-1H-pyrazole-4-carbaldehyde can participate in various organic reactions such as condensation, nucleophilic addition, and cycloaddition reactions. Its presence in a synthetic pathway can lead to the formation of structurally complex molecules with potential applications in medicinal chemistry and material science.Overall, the application of 1-(3-Fluorophenyl)-1H-pyrazole-4-carbaldehyde in chemical synthesis underscores its significance as a valuable intermediate for the preparation of diverse compounds with potential pharmaceutical, agricultural, and industrial applications.