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Pirazol

Pirazol
Formula kimikoaC3H4N2
SMILES kanonikoa2D eredua
MolView3D eredua
KonposizioaNitrogeno eta karbono
MotaAlkaloide eta konposatu heterozikliko
Tautomeroa3H-pyrazole (en) Itzuli eta 4H-pyrazole (en) Itzuli
Ezaugarriak
Fusio-puntua68 ℃
Irakite-puntua187 ℃ (101,325 kPa)
Masa molekularra68,037 Da
Erabilera
RolaEntzimen inhibitzaile
Identifikatzaileak
InChlKeyWTKZEGDFNFYCGP-UHFFFAOYSA-N
CAS zenbakia288-13-1
ChemSpider1019
PubChem1048
Reaxys103775
Gmelin17241
ChEBI1360
ChEMBLCHEMBL15967
RTECS zenbakiaUQ4900000
ZVG492981
DSSTox zenbakiaUQ4900000
EC zenbakia206-017-1
ECHA100.005.471
MeSHC031280
Human Metabolome DatabaseHMDB0256947
UNII3QD5KJZ7ZJ
KEGGC00481
PDB LigandPZO

Pirazola C3H4N2 formula duen bost begiko heterozikloa da non bi nitrogeno-atomoak elkarren ondoan dauden. Halaber, eraztunaren deribatu ordezkatuen familiari esaten zaie pirazol[1].

Base ahula da.

Botika askok pirazol-eraztuna dute egituran hala nola zelecoxib antiflamatorioak edo estranozolol esteroide anabolizanteak. Herbiziden egituretan ere ageri dira pirazol-eraztunak.

Sintesia

Pirazolak aldehido α,ß-asegabea hidrazinarekin tratatuz sintetizatze dira[2].

Erreferentziak

  1. ↑ Eicher, Theophil. (2003). The chemistry of heterocycles : structure, reactions, syntheses, and applications. (2nd, completely rev., and enl. ed. argitaraldia) Wiley-VCH ISBN 3-527-30720-6. PMC 52784213. (kontsulta data: 2022-11-20).
  2. ↑ (Ingelesez) Schmidt, Andreas; Dreger, Andrij. «Recent Advances in the Chemistry of Pyrazoles. Properties, Biological Activities, and Syntheses» Current Organic Chemistry 15 (9): 1423–1463. (kontsulta data: 2022-11-20).

Kanpo estekak

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