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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)-

4-iodo-2-methylpyrazole-3-carbaldehyde

Cn1ncc(c1C=O)I Request for Quotation
Chemical Name: 4-iodo-2-methylpyrazole-3-carbaldehyde
CAS Number: 959986-66-4
Product Number: AG005W0R(AGN-PC-01MJR0)
Synonyms:
MDL No:
Molecular Formula: C5H5IN2O
Molecular Weight: 236.0105

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.012g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
235.945g/mol
Monoisotopic Mass:
235.945g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
120
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Iodo-1-methyl-1H-pyrazole-5-carbaldehyde is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound is commonly employed as a key building block in the production of pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, 4-Iodo-1-methyl-1H-pyrazole-5-carbaldehyde serves as a valuable intermediate for the synthesis of complex organic molecules. Its structure contains functional groups that allow for various chemical transformations, making it an essential component in the preparation of diverse compounds.This compound is particularly useful in the modification of heterocyclic scaffolds and the introduction of specific functional groups into target molecules. Its reactivity enables selective reactions that facilitate the creation of novel compounds with important biological and chemical properties.Furthermore, 4-Iodo-1-methyl-1H-pyrazole-5-carbaldehyde plays a crucial role in the development of new materials with specialized functions, such as molecular probes, fluorescence dyes, and pharmaceutical intermediates. Its presence in the molecular structure imparts specific characteristics to the final products, enhancing their utility in various applications.Overall, the strategic utilization of 4-Iodo-1-methyl-1H-pyrazole-5-carbaldehyde in chemical synthesis enables the efficient and precise construction of valuable molecules with diverse functionalities and applications.