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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-ethylpyrazole-3-carbaldehyde

O=Cc1ccn(n1)CC Request for Quotation
Chemical Name: 1-ethylpyrazole-3-carbaldehyde
CAS Number: 942319-16-6
Product Number: AG00604N(AGN-PC-0LW8L7)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O
Molecular Weight: 124.1405

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
124.143g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
124.064g/mol
Monoisotopic Mass:
124.064g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
105
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-Ethyl-1H-pyrazole-3-carbaldehyde is a key compound used in chemical synthesis as a versatile building block for the creation of diverse organic molecules. Its unique structure and reactivity make it an important tool for chemists in the development of various pharmaceuticals, agrochemicals, and materials.One of the prominent applications of 1-Ethyl-1H-pyrazole-3-carbaldehyde is its role as a precursor in the synthesis of heterocyclic compounds. By undergoing various chemical transformations, this compound can be used to introduce functional groups and modify the properties of the final products. Its ability to participate in reactions such as condensations, cycloadditions, and metal-catalyzed cross-coupling reactions allows for the construction of complex structures with high efficiency.Furthermore, 1-Ethyl-1H-pyrazole-3-carbaldehyde serves as a valuable scaffold for the design and development of bioactive molecules. Its presence in the structure of drug candidates can impart desirable pharmacological properties or improve the overall efficacy of the compound. Chemists leverage the versatility of this compound to create analogs and derivatives that exhibit enhanced biological activities or improved pharmacokinetic profiles.Overall, the strategic use of 1-Ethyl-1H-pyrazole-3-carbaldehyde in chemical synthesis enables researchers to access a wide range of molecular architectures with potential applications in medicinal chemistry, materials science, and other specialized fields.