1202873-59-3

Basic information

• Product Name: 3-(4-tert-butylphenyl)-1-methyl-1H-pyrazol-5-ol
• CAS NO: 1202873-59-3
• Molecular Weight: 230.31
• Mol File: 1202873-59-3.mol

Chemical Properties

• CAS DataBase Reference: 3-(4-tert-butylphenyl)-1-methyl-1H-pyrazol-5-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-tert-butylphenyl)-1-methyl-1H-pyrazol-5-ol(1202873-59-3)
• EPA Substance Registry System: 3-(4-tert-butylphenyl)-1-methyl-1H-pyrazol-5-ol(1202873-59-3)

Safety Data

• Hazardous Substances Data: 1202873-59-3(Hazardous Substances Data)

Upstream product

• 200280-57-5 methyl 3-(4-(tert-butyl)phenyl)-3-oxopropanoate 
• 60-34-4 methylhydrazine 
• 943-27-1 4'-t-butylacetophenone 

Downstream Products

• 1097726-55-0 C₂₅H₃₀N₄O₃ 

Relevant articles and documents

PYRAZOLONE DERIVATIVES AS NITROXYL DONORS

The disclosed subject matter provides pyrazolone derivative compounds, pharmaceutical compositions comprising such compounds, kits comprising such compounds, and methods of using such compounds or pharmaceutical compositions. In particular, the disclosed subject matter provides methods of using such compounds or pharmaceutical compositions for treating heart failure.

Synthesis and biological activity of new (E)-α-(Methoxyimino) benzeneacetate derivatives containing a substituted pyrazole ring

Strobilurins are one of the most important classes of agricultural fungicides. To discover new strobilurin analogues with high activity, a series of new strobilurin derivatives containing a substituted pyrazole in the side chain were synthesized and their biological activities were tested. The compounds were identified by 1H nuclear magnetic resonance, infrared, and elemental analysis. The test results indicated that the compounds exhibited strong fungicidal activities against Pyricularia oryzae, Phytophthora infestans, Pseudoperonospora cubenssi, and Erysiphe graminis. The relationship between structure and biological activity is discussed in terms of the effects of the substituents on the pyrazole ring. The present work demonstrates that strobilurin analogues with a 3-(substituted phenyl)-1 H-pyrazol-5-oxy side chain can be used as possible lead compounds for the development of potential agrochemicals.