5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one

• CAS: 89-25-8
• Catalog Number: ACM89258
• Category: Other Products
• Molecular Weight: 174.2
• Molecular Formula: C₁₀H₁₀N₂O
• Synonyms: TIMTEC-BB SBB003801;PMP;MONOPYRAZOLONE;MCI-186;EDARAVONE;C.I. Developer 1;AURORA KA-3365;2,4-dihydro-5-methyl-2-phenyl-3h-pyrazol-3-one
• Boiling Point: 287°C265mm Hg(lit.)
• Melting Point: 126-128°C(lit.)
• Flash Point: 191°C/17mm
• Density: 1,12 g/cm³
• Hazard Statements: Xi
• Safety Description: 26-36
• Supplemental Hazard Statements: H303-H302-H315-H319-H335
• Symbol: GHS07

Custom Q&A

What is the molecular formula of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one?

The molecular formula is C10H10N2O.

What is the molecular weight of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one?

The molecular weight is 174.20 g/mol.

What is the IUPAC name of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one?

The IUPAC name is 5-methyl-2-phenyl-1H-pyrazol-3-one.

What is the InChI of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one?

The InChI is InChI=1S/C10H10N2O/c1-8-7-10(13)12(11-8)9-5-3-2-4-6-9/h2-7,11H,1H3.

What is the InChIKey of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one?

The InChIKey is KZQYIMCESJLPQH-UHFFFAOYSA-N.

What is the canonical SMILES of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one?

The canonical SMILES is CC1=CC(=O)N(N1)C2=CC=CC=C2.

What is the CAS number of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one?

The CAS numbers are 19735-89-8 and 942-32-5.

How many hydrogen bond donor counts does 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one have?

It has 1 hydrogen bond donor count.

How many hydrogen bond acceptor counts does 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one have?

It has 2 hydrogen bond acceptor counts.

Synthetic Use

Downstream Synthesis Route 1

• 54660-80-9
• 89-25-8

• 6642-31-5
• 4702-90-3

Reference: [1] Synlett, 2009, # 12, p. 1982 - 1984

Downstream Synthesis Route 2

• 89-25-8

• 1128-54-7

Reference: [1] Justus Liebigs Annalen der Chemie, 1887, vol. 238, p. 213

Downstream Synthesis Route 3

• 89-25-8
• 35824-85-2

• 6972-27-6
• 4702-90-3

Reference: [1] Synlett, 2009, # 12, p. 1982 - 1984

Downstream Synthesis Route 4

• 89-25-8

• 1128-54-7

Reference: [1]Justus Liebigs Annalen der Chemie,1887,vol. 238,p. 213

* For details of the synthesis route, please refer to the original source to ensure accuracy.