10250-62-1

Basic information

• Product Name: 1-Methyl-3-phenylpyrazol-5-carbonsaeure-methylester
• Synonyms: 1-Methyl-3-phenylpyrazol-5-carbonsaeure-methylester
• CAS NO: 10250-62-1
• Molecular Formula: C₁₂H₁₂N₂O₂
• Molecular Weight: 232.23528
• EINECS: -0
• Mol File: 10250-62-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Methyl-3-phenylpyrazol-5-carbonsaeure-methylester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methyl-3-phenylpyrazol-5-carbonsaeure-methylester(10250-62-1)
• EPA Substance Registry System: 1-Methyl-3-phenylpyrazol-5-carbonsaeure-methylester(10250-62-1)

Safety Data

• Hazardous Substances Data: 10250-62-1(Hazardous Substances Data)

Usage

Methyl ester derivative

1-Methyl-3-phenylpyrazole-5-carboxylic acid Indicates that the compound is derived from 1-methyl-3-phenylpyrazole-5-carboxylic acid by replacing the carboxylic acid group (-COOH) with a methyl ester group (-COOCH3).

Industries and research applications

Pharmaceutical and agrochemical The compound is used in various industries, including the production of pharmaceuticals and agrochemicals.

Physical appearance

White to off-white solid Describes the color and form of the compound when in its pure state.

Melting point

118-119°C The temperature range at which the compound transitions from a solid to a liquid state.

Solubility

Insoluble in water, soluble in organic solvents Indicates the compound's solubility behavior in different solvents, which can be important for its handling and application.

Chemical structure and properties

Useful for potential biological activities and synthesis of other organic compounds The compound's structure and properties make it a valuable building block for creating other organic compounds and for potential biological activities in research and applications.

Upstream product

• 98-86-2 acetophenone 
• 90145-13-4 N'-<α-bromobenzylidene>-N-methylhydrazinium bromide 
• 922-67-8 propynoic acid methyl ester 
• 56426-35-8 methyl 5-phenyl-1H-pyrazole-3-carboxylate 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 
• 60-29-7 diethyl ether 
• 60-34-4 methylhydrazine 
• 20577-73-5 methyl 4-phenyl-2,4-dioxobutanoate 
• 13466-29-0 1-benzylidene-2-methylhydrazine 
• 90145-20-3 1-Methyl-3-phenyl-2-pyrazolin-5-carbonsaeure-methylester 

Downstream Products

• 10250-64-3 2-Methyl-5-phenyl-2H-pyrazole-3-carboxylic acid 

Relevant articles and documents

AMIDE COMPOUNDS

The present invention provides compounds represented by the formula (Ia) the formula (Ib) the formula (Ic) and the formula (Id) wherein each symbol is as defined in the specification. According to the present invention, these compounds have a DGAT inhibit

1,3-Dipolar Cycloadditions, 91. The Chemistry of N-Methyl-C-phenylnitrilimine

The treatment of N'--N-methylhydrazinium bromide, accessible by bromination of benzaldehyde-N-methylhydrazone, with triethylamine furnishes the title compound; this method is superior to the thermolysis and photolysis of 2-methyl-5-phe