3784-97-2 Usage
Explanation
The compound consists of 8 carbon atoms, 9 hydrogen atoms, 1 nitrogen atom, and 1 oxygen atom.
Explanation
The compound is derived from 1-methyl-1,2-dihydropyridine by attaching a carbonyl group (C=O) to the second carbon atom.
Explanation
The presence of the carbonyl group (C=O) makes it an aldehyde.
Explanation
1-methyl-1,2-dihydropyridine-2-carbaldehyde is commonly used as an intermediate in the production of various types of pyridine derivatives, which are important in pharmaceuticals.
Explanation
The compound can be used to impart specific flavors to food and beverages.
Explanation
1-methyl-1,2-dihydropyridine-2-carbaldehyde can be employed as a reagent in certain organic chemistry reactions, aiding in the synthesis or modification of other compounds.
Structure
1-methyl-1,2-dihydropyridine derivative with a carbonyl group
Type
Aldehyde
Industrial applications
Synthesis of pharmaceuticals
Use as flavoring agent
Food and beverage industry
Use as a reagent
Organic chemistry reactions
Check Digit Verification of cas no
The CAS Registry Mumber 3784-97-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3784-97:
(6*3)+(5*7)+(4*8)+(3*4)+(2*9)+(1*7)=122
122 % 10 = 2
So 3784-97-2 is a valid CAS Registry Number.
3784-97-2Relevant articles and documents
Kinetics of Hydrolysis of Some New Heterocyclic Azomethines
Mahmoud, Mohamed Rafat,Hamed, Maher Mohamed Ahmed,Shaker, Ali Mohamed
, p. 765 - 776 (2007/10/02)
Kinetics of base hydrolysis of new heterocyclic azomethines derived from active methyl quaternary salts and aromatic nitroso compounds were investigated in the presence of 70percent (wt/wt) water-methanol.The base hydrolysis of these compounds is strictly first-order with respect to OH- and azomethine.The rate determining step is suggested to be the attack of the hydroxide ion on the free base.Effects of water content and nature of organic hydroxylic solvent have been studied.It is concluded that specific solute-solvent interactions through dispersion forces play a major role in the base hydrolysis rate of the azomethines investigated.The effect of pH (2.98 - 12.24) on hydrolysis rates of compounds having a diethylamino substituent in the presence of 30percent methanol has been studied.In acidic media, the rate determining step is probably the water attack on the protonated substrate.
