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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)-

ethyl 5-chloro-1H-pyrazole-4-carboxylate

CCOC(=O)c1cn[nH]c1Cl Request for Quotation
Chemical Name: ethyl 5-chloro-1H-pyrazole-4-carboxylate
CAS Number: 948552-01-0
Product Number: AG00IKKS(AGN-PC-04Q5L3)
Synonyms:
MDL No:
Molecular Formula: C6H7ClN2O2
Molecular Weight: 174.58498

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 5-chloro-1H-pyrazole-4-carboxylate is a versatile chemical compound that finds important applications in organic synthesis. With its unique molecular structure, this compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals.In chemical synthesis, Ethyl 5-chloro-1H-pyrazole-4-carboxylate can be utilized as a key intermediate in the development of biologically active compounds. Its functional groups and reactivity make it suitable for the formation of complex molecular structures through derivatization and further functionalization. This compound can participate in a variety of reactions such as nucleophilic substitution, esterification, and cyclization, allowing for the efficient creation of diverse chemical entities.Furthermore, Ethyl 5-chloro-1H-pyrazole-4-carboxylate acts as a valuable precursor in the synthesis of heterocyclic compounds, which are prevalent in the pharmaceutical industry due to their diverse biological activities. By incorporating this compound into synthetic pathways, chemists can access a wide range of pharmacologically significant molecules with potential therapeutic benefits.Overall, the application of Ethyl 5-chloro-1H-pyrazole-4-carboxylate in chemical synthesis enables the synthesis of novel compounds with enhanced properties and biological activities, showcasing its significance in the field of organic chemistry and drug discovery.