4808-75-7

Usage

Uses

Used in Pharmaceutical Industry:
3,5-DIETHYL-2-N-PROPYLPYRIDINE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs. Its unique chemical structure allows for the creation of diverse medicinal compounds with potential therapeutic applications.
Used in Organic Chemistry:
3,5-DIETHYL-2-N-PROPYLPYRIDINE is used as a reagent and building block in organic chemistry for its capacity to participate in a range of chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Agricultural Applications:
In the agricultural sector, 3,5-DIETHYL-2-N-PROPYLPYRIDINE is used as a component in the formulation of certain agrochemicals, potentially contributing to pest control or crop enhancement strategies.
Used in Industrial Applications:
3,5-DIETHYL-2-N-PROPYLPYRIDINE finds use in various industrial processes, where its chemical properties may be leveraged for the production of specialty chemicals or materials.

InChI:InChI=1/C12H19N/c1-4-7-12-11(6-3)8-10(5-2)9-13-12/h8-9H,4-7H2,1-3H3

Upstream product

• 40898-95-1 1-(-)-2-amino-1-butanol 
• 123-72-8 butyraldehyde 
• 41808-04-2 2r,4c,6c-tripropyl-hexahydro-[1,3,5]triazine 
• 872-85-5 pyridine-4-carbaldehyde 
• 98-01-1 furfural 
• 555-16-8 4-nitrobenzaldehdye 
• 100-52-7 benzaldehyde 
• 90-02-8 salicylaldehyde 
• 446-52-6 2-Fluorobenzaldehyde 
• 135-02-4 ortho-anisaldehyde 
• 7664-41-7 ammonia 
• 60-29-7 diethyl ether 
• 64-17-5 ethanol 
• 82166-21-0 methyl cyclohexane 

Relevant academic research and scientific papers

Mesoporous Aluminosilicates in the Synthesis of N-Heterocyclic Compounds

Abstract: The catalytic properties of samples of amorphous mesoporous aluminosilicate ASM with different Si/Al molar ratios (40, 80, 160) were studied in the synthesis of practically important pyridines (by the interaction of С2–С5 alcohols with formaldehyde and ammonia, cyclocondensation of acetaldehyde and propionic aldehyde with ammonia), dialkylquinolines and alkyltetrahydroquinolines (by reaction of aniline with C3, C4 aldehydes) and alkyldihydroquinolines (by interaction of aniline with ketones, acetone and acetophenone). It is found that mesoporous aluminosilicate ASM sample with a molar ratio of Si/Al = 40, which has the highest acidity among the studied samples, exhibits the highest activity and selectivity in these reactions.

Substituted pyridines and dihydropyridines

This invention relates to a process of preparing alkylpyridines and N-substituted alkyldihydropyridines from hexahydrotriazines. These products may be further reacted to form other compositions. The products of the reaction are useful as corrosion inhibitors.

Triazolo[4,3-d][1,4]benzodiazepine-6-ones

Compounds having the structure STR1 wherein R1 is hydrogen, alkyl, phenyl, or benzyl; R2 is hydrogen or alkyl; R3 is hydrogen, alkyl, haloalkyl, cyanoalkyl, trifluoromethyl, phenyl, benzyl, STR2 OR --(CH2)n --NR5 R6 ; R4 is hydrogen, halogen, nitro, cyano, trifluoromethyl, alkyl, alkoxy, or alkylthio; R5 and R6 are the same or different and are hydrogen or alkyl or R5 and R6 together with the nitrogen atom to which they are attached form a five or six membered heterocyclic ring; and n is 1, 2, 3 or 4; are useful as anti-inflammatory agents.

Conversion of tetrahydropyrimidines to pyridines

A process of converting 2,3,4,5-tetrahydropyrimidines containing at least 1 hydrogen in the 2-position and at least one methylene group in the 4-position to corresponding pyridines which comprises heating said tetrahydropyrimidines to a temperature sufficiently high to remove ammonia and hydrogen so as to form said pyridines.