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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)-

benzyl 4-iodopyrazole-1-carboxylate

Ic1cnn(c1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: benzyl 4-iodopyrazole-1-carboxylate
CAS Number: 952338-83-9
Product Number: AG00IIVN(AGN-PC-0I4PFK)
Synonyms:
MDL No:
Molecular Formula: C11H9IN2O2
Molecular Weight: 328.10583

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzyl 4-iodo-1H-pyrazole-1-carboxylate is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various organic molecules. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique reactivity and structural properties.In chemical synthesis, Benzyl 4-iodo-1H-pyrazole-1-carboxylate can be employed as a precursor for the introduction of the pyrazole ring system into complex organic molecules. The presence of the iodo functional group enables cross-coupling reactions, such as Suzuki-Miyaura coupling or Sonogashira coupling, to facilitate the formation of new carbon-carbon bonds. This reactivity allows for the efficient modification and functionalization of the pyrazole core, enabling the creation of diverse compound libraries for drug discovery and material science applications.Furthermore, the benzyl ester moiety in Benzyl 4-iodo-1H-pyrazole-1-carboxylate can serve as a protecting group, providing selectivity in chemical transformations and allowing for the controlled modification of the molecule under specific reaction conditions. By strategically removing the benzyl protecting group at different stages of the synthesis, chemists can access multiple intermediates with varying functionalities, leading to the efficient synthesis of complex molecules with tailored properties.Overall, Benzyl 4-iodo-1H-pyrazole-1-carboxylate plays a crucial role in chemical synthesis by enabling the construction of structurally diverse compounds with potential applications in drug development, material science, and other fields requiring the synthesis of complex organic molecules.