1163-71-9 Usage
Description
2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone is a chemical compound synthesized by the reaction of 2-methoxybenzaldehyde with 2,4-dinitrophenyl hydrazine. It is characterized by its yellow crystalline appearance and a distinct strong odor. 2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone is primarily recognized for its role as a reagent in organic synthesis, particularly in the identification and analysis of carbonyl compounds through the formation of colored precipitates.
Uses
Used in Organic Synthesis:
2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone is used as a reagent in organic synthesis for its ability to facilitate the detection and analysis of carbonyl compounds. It aids in the formation of colored precipitates, which is instrumental in the identification process.
Used in Analytical Chemistry:
In the field of analytical chemistry, 2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone is employed as an analytical reagent for the determination of aldehydes and ketones in various samples. Its capacity to produce colored precipitates upon reaction with these compounds makes it a valuable tool for qualitative and quantitative analysis.
Used in Antimicrobial Research:
2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone has been studied for its potential antimicrobial properties, indicating its possible use in the development of new antimicrobial agents or treatments.
Used in Antioxidant Research:
2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone is also being investigated for its antioxidant properties, which could lead to its application in the development of antioxidants for various industrial or medicinal uses.
Used in Pharmaceutical Industry:
Given its potential antimicrobial and antioxidant properties, 2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone could be utilized in the pharmaceutical industry for the development of new drugs or supplements.
Safety Note:
It is crucial to handle 2-Methoxybenzaldehyde 2,4-dinitrophenyl hydrazone with care due to its toxic nature. Ingestion, inhalation, or skin and eye contact can cause irritation or more severe health effects, necessitating proper safety measures during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 1163-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1163-71:
(6*1)+(5*1)+(4*6)+(3*3)+(2*7)+(1*1)=59
59 % 10 = 9
So 1163-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N4O5/c1-23-14-5-3-2-4-10(14)9-15-16-12-7-6-11(17(19)20)8-13(12)18(21)22/h2-9,16H,1H3/b15-9+
1163-71-9Relevant articles and documents
Structure-Reactivity correlation in the oxidation of substituted benzaldehydes by tetraethylammonium chlorochromate
Gehlot,Prasadrao,Sharma
experimental part, p. 1173 - 1178 (2012/01/05)
Oxidation of 36 monosubstituted benzaldehydes by tetraethylammonium chlorochromate in dimethyl sulphoxide, leads to the formation of corresponding benzoic acids. The reaction is of first order with respect to chlorochromate and aldehydes. The reaction is promoted by H+; the H+ dependence has the form kobs = a + b[H+]. The oxidation of duteriated benzaldehyde exhibits substantial primary kinetic isotope effect. The reaction was studied in 19 different organic solvents and the effect of solvent was analyzed using Taft's and Swain's multiparametric equations. The rates of the oxidation of para- and meta-substituted benzaldehydes showed excellent correlation in terms of Charton's triparametric LDR equation, whereas the oxidation of ortho-substituted benzaldehydes were correlated well with tetraperametric LDRS equation. The oxidation of para-substituted benzaldehydes is more susceptible to the delocalized effect than is the oxidation of ortho- and meta- substituted compounds, which display a greater dependence on the field effect. The positive value of h suggests the presence of an electron-deficient reaction centre in the rate-determining step. The reaction is subjected to steric acceleration by the orthosubstituents. A suitable mechanism has been proposed.
