788797-92-2 Usage
Methyl ester derivative
phenylhydrazinecarboxylic acid The compound is derived from phenylhydrazinecarboxylic acid by replacing the carboxylic acid group (-COOH) with a methyl ester group (-COOCH3).
Physical appearance
pale yellow solid The compound appears as a pale yellow solid in its pure form.
Solubility
organic solvents (ethanol, acetone) 1-phenylHydrazinecarboxylic acid methyl ester is soluble in organic solvents such as ethanol and acetone, which means it can dissolve in these solvents to form a homogeneous solution.
Common uses
organic synthesis, pharmacological research The compound is commonly used in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals, as well as in pharmacological research.
Safety precautions
harmful if ingested or inhaled, skin and eye irritation Handling this compound requires care, as it may be harmful if ingested or inhaled and may cause irritation to the skin and eyes upon contact.
Storage conditions
cool, dry place, away from direct sunlight and heat sources To maintain the stability and safety of the compound, it should be stored in a cool, dry place, away from direct sunlight and heat sources.
Check Digit Verification of cas no
The CAS Registry Mumber 788797-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,8,7,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 788797-92:
(8*7)+(7*8)+(6*8)+(5*7)+(4*9)+(3*7)+(2*9)+(1*2)=272
272 % 10 = 2
So 788797-92-2 is a valid CAS Registry Number.
788797-92-2Relevant articles and documents
Reaction of the ambident electrophile dimethyl carbonate with the ambident nucleophile phenylhydrazine
Rosamilia, Anthony E.,Arico, Fabio,Tundo, Pietro
, p. 1559 - 1562 (2008/09/17)
(Chemical Equation Presented) To explore the ambident electrophilic reactivity of dimethyl carbonate (DMC), reactions with the ambident nucleophile phenylhydrazine were investigated. When a Broensted base was used, selective carboxymethylation occurred at
QUINOLINE DERIVATIVES AS NEUROKININ RECEPTOR ANTAGONISTS
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Page/Page column 27, (2008/06/13)
The present invention relates to substituted quinoline-4-carboxylic acid hydrazides defined herein, pharmaceutical compositions comprising them and their use in treating diseases mediated by neurokinin-2 and/or neurokinin-3 (NK-3) receptors.
