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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)-

3H-Pyrazol-3-one,4-butyl-4-Butyl-3-hydroxy-1-(4-hydroxyphenyl)-2-phenyl-3-pyrazolin-5-one

CCCCc1c(=O)n(n(c1O)c1ccccc1)c1ccc(cc1)O Request for Quotation
Chemical Name: 3H-Pyrazol-3-one,4-butyl-4-Butyl-3-hydroxy-1-(4-hydroxyphenyl)-2-phenyl-3-pyrazolin-5-one
CAS Number: 975-18-8
Product Number: AG005ZAS(AGN-PC-0W77FK)
Synonyms:
MDL No:
Molecular Formula: C19H20N2O3
Molecular Weight: 324.3737

Identification/Properties

Properties
BP:
503.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 4-Butyl-5-hydroxy-2-(4-hydroxyphenyl)-1-phenyl-1H-pyrazol-3(2H)-one is a versatile compound commonly used as a building block for the creation of complex organic molecules. This compound serves as a key intermediate in the development of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. Its presence in chemical reactions can lead to the formation of diverse functional groups and intricate molecular frameworks, making it a valuable tool for synthetic chemists aiming to design and produce novel compounds with specific properties and applications. The strategic incorporation of 4-Butyl-5-hydroxy-2-(4-hydroxyphenyl)-1-phenyl-1H-pyrazol-3(2H)-one in synthesis routes allows for the controlled modification and functionalization of organic molecules, enabling the tailored production of desired products with enhanced physicochemical characteristics and biological activities.