10250-62-1 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.
Check Digit Verification of cas no
The CAS Registry Mumber 10250-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10250-62:
(7*1)+(6*0)+(5*2)+(4*5)+(3*0)+(2*6)+(1*2)=51
51 % 10 = 1
So 10250-62-1 is a valid CAS Registry Number.
10250-62-1Relevant articles and documents
AMIDE COMPOUNDS
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Page/Page column 259-260, (2008/06/13)
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
Fliege, Werner,Grashey, Rudolf,Huisgen, Rolf
, p. 1194 - 1214 (2007/10/02)
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