39513-12-7

Basic information

• Product Name: 1H-Pyrazole, 3-methoxy-4-methyl-5-phenyl-
• CAS NO: 39513-12-7
• Molecular Formula: C11H12N2O
• Molecular Weight: 188.229
• Mol File: 39513-12-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Pyrazole, 3-methoxy-4-methyl-5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole, 3-methoxy-4-methyl-5-phenyl-(39513-12-7)
• EPA Substance Registry System: 1H-Pyrazole, 3-methoxy-4-methyl-5-phenyl-(39513-12-7)

Safety Data

• Hazardous Substances Data: 39513-12-7(Hazardous Substances Data)

Upstream product

• 87389-78-4 2-amino-4-methyl-5-phenyl-1,2-dihydro-pyrazol-3-one 
• 39513-01-4 1-amino-5-methoxy-4-methyl-3-phenylpyrazole 
• 142310-44-9 1-<(1-phenylethylidene)amino>-3-methoxy-4-methyl-5-phenylpyrazole 
• 142310-41-6 1-<(1-phenylethylidene)amino>-3-phenyl-4-methyl-5-hydroxypyrazole 
• 142310-43-8 1-amino-3-methoxy-4-methyl-5-phenylpyrazole 
• 142310-28-9 1-<1-(4-biphenylethylidene)amino>-3-phenyl-4-methyl-5-methoxypyrazole 
• 142310-26-7 1-<(diphenylmethylene)amino>-3-phenyl-4-methyl-5-methoxypyrazole 
• 142310-45-0 1-<(1-phenylethyl)amino>-3-methoxy-4-methyl-5-phenylpyrazole 
• 142310-25-6 1-<(1-phenylethylidene)amino>-3-phenyl-4-methyl-5-methoxypyrazole 
• 142310-27-8 1-<(1-cyclohexylidene)amino>-3-phenyl-4-methyl-5-methoxypyrazole 
• 142310-24-5 1-<(1-methylpropylidene)amino>-3-phenyl-4-methyl-5-methoxypyrazole 
• 142310-23-4 1-(isopropylidene)amino-3-phenyl-4-methyl-5-methoxypyrazole 

Downstream Products

• 1239915-34-4 dimethyl 2-(5-methoxy-4-methyl-3-phenyl-1H-pyrazol-1-ylimino)succinate 
• 142310-45-0 1-<(1-phenylethyl)amino>-3-methoxy-4-methyl-5-phenylpyrazole 
• 142310-44-9 1-<(1-phenylethylidene)amino>-3-methoxy-4-methyl-5-phenylpyrazole 
• 142310-43-8 1-amino-3-methoxy-4-methyl-5-phenylpyrazole 

Relevant articles and documents

Hydrogenolysis of 1-Aminopyrazoles: Synthesis of Primary and Secondary Alkylamines

The tautomerizable N-aminopyrazolone 9, the O-methyl 1 and N-methyl derivatives 4 were condensed with carbonyl compounds to give the alkenylaminopyrazoles 12, 2a-g and 5c, wich, under mild conditions, were hydrogenated to the corresponding alkylamino derivatives.The subesquent hydrogenation of the latter ones gave different results according to the structure of the starting material.The 5-methoxy-1-alkylaminopyrazoles 3a-g yielded the 5-methoxypyrazole 15 and the corresponding primary amines in good yields.On the contrary, N-methyl-1-alkylaminopyrazolone-5 6c gave 1-a lkylpyrazolone-3 8.