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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)-

1H-Imidazole-5-carboxaldehyde, 1-ethyl-

O=Cc1cncn1CC Request for Quotation
Chemical Name: 1H-Imidazole-5-carboxaldehyde, 1-ethyl-
CAS Number: 842972-42-3
Product Number: AG004TI0(AGN-PC-0KPYSM)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O
Molecular Weight: 124.1405

Identification/Properties

Computed Properties
Molecular Weight:
124.143g/mol
XLogP3:
0.1
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Ethyl-1H-imidazole-5-carbaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential reagent in the field of organic chemistry.In chemical synthesis, 1-Ethyl-1H-imidazole-5-carbaldehyde acts as a valuable intermediate in the preparation of heterocyclic compounds, particularly imidazole derivatives. Its presence allows for the introduction of functional groups and modifications that are essential for fine-tuning the properties of the final product. The aldehyde group in this compound also serves as a versatile functional handle for further transformations, enabling the creation of a diverse range of complex molecules.Furthermore, 1-Ethyl-1H-imidazole-5-carbaldehyde can serve as a key starting material in the synthesis of bioactive compounds, such as pharmaceuticals and biologically active substances. Its ability to participate in various organic reactions, such as condensations, reductions, and transformations, makes it a valuable tool for chemists seeking to design and produce novel molecules with specific pharmacological properties.Overall, the application of 1-Ethyl-1H-imidazole-5-carbaldehyde in chemical synthesis is instrumental in expanding the repertoire of available compounds and driving innovation in drug discovery, materials science, and other chemical industries.