116314-34-2 Usage
Cyanobenzoate derivative
A derivative of cyanobenzoic acid This indicates that the compound is derived from cyanobenzoic acid by modifying its structure.
Butyl group attached to the 1-position
The butyl group (C4H9) is attached to the first carbon atom of the cyanobenzoate core This describes the specific location of the butyl group on the molecule.
Commonly used in synthesis of pharmaceuticals and agrochemicals
The compound serves as an intermediate or building block in the production of drugs and agrochemicals This highlights the compound's practical applications in various industries.
Potential antioxidant and anti-inflammatory properties
The compound may have the ability to reduce oxidative stress and inflammation This suggests possible therapeutic uses for the compound in drug development.
Desirable candidate for drug development
Due to its potential properties, the compound is a promising candidate for further research and development in the pharmaceutical industry This emphasizes the compound's potential for future applications.
Unique structure
The compound has a distinct arrangement of functional groups and atoms This may contribute to its usefulness in various chemical reactions and applications in organic chemistry.
Further research needed
More studies are required to fully understand the compound's potential uses and effects This acknowledges that the compound's full potential has not yet been explored and that additional research is necessary.
Check Digit Verification of cas no
The CAS Registry Mumber 116314-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,1 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116314-34:
(8*1)+(7*1)+(6*6)+(5*3)+(4*1)+(3*4)+(2*3)+(1*4)=92
92 % 10 = 2
So 116314-34-2 is a valid CAS Registry Number.
116314-34-2Relevant academic research and scientific papers
PHARMACOLOGICALLY ACTIVE COMPOUNDS, METHODS FOR THE PREPARATION THEREOF AND COMPOSITIONS CONTAINING THE SAME
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, (2008/06/13)
Pharmacologically active catechol derivatives of formula I I wherein R1 and R2 independently comprise hydrogen, alkyl, acyl, optionally substituted aroyl, lower alkylsulfonyl or alkylcabamoyl or taken together form a lower alkylidene or cycloalkylidene, X comprises an electronegative substituent such as halogen, nitro, cyano, lower alkylsulfonyl, sulfonamido, aldehyde, caboxyl or trifluoromethyl and R3 comprises hydrogen, halogen, hydroxy alkyl, amino, nitro, cyano, trifluoromethyl, lower alkylsulfonyl, sulfonamide, aldehyde, alkyl carbonyl, aralkylidene carbonyl or carboxyl or a group selected from wherein R4 comprises hydrogen, alkyl, cyano, carboxyl or acyl and R5 comprises hydrogen, cyano, carboxyl, alkoxycarbonyl, carboxyalkenyl, nitro, acyl, optionally substituted aroyl or heteroaroyl, hydroxyalkyl or carboxyalkyl or R4 and R5 together form a five to seven membered substituted cycloalkanone ring; -(CO)n(CH2)m-COR wherein n is 0-1 and m is 0-7 and R comprises hydroxy, alkyl, carboxyalkyl, optionally substituted alkene, alkoxy or optionally substituted amino; wherein R8 and R9 independently comprise hydrogen or one of the following optionally substituted groups; alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl, or together form an optionally substituted piperidyl group; -NH-CO-R10 wherein R10 comprises a substituted alkyl group
