6295-64-3

Usage

Molecular structure

A complex organic compound with a quinoline-4-carboxylate core, ethyl and phenyl groups, chloro-nitrophenyl, and dioxooctahydro-2H-4,7-methanoisoindol-2-yl groups.

Molecular weight

617.07 g/mol

Appearance

Potentially a solid or crystalline substance, though the exact appearance is not provided.

Solubility

The solubility properties are not provided, but it may be soluble in organic solvents like ethanol or acetone.

Stability

The stability of the compound is not explicitly mentioned, but it may be sensitive to certain conditions such as heat, light, or moisture.

Reactivity

The reactivity of the compound is not provided, but the presence of various functional groups (e.g., chloro, nitro, and carbonyl) suggests that it may undergo various chemical reactions.

Potential applications

2-(4-chloro-3-nitrophenyl)-2-oxoethyl 2-[4-(1,3-dioxooctahydro-2H-4,7-methanoisoindol-2-yl)phenyl]quinoline-4-carboxylate may have applications in pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties.

Further research

Additional research and testing are required to fully understand the potential uses and effects of this complex chemical compound.

Upstream product

• 105-31-7 1-hexyn-3-ol 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 57189-00-1 propargylic tert-butoxy ether 

Downstream Products

• 54123-75-0 3-hydroxy-2-hexanone 
• 105-31-7 (S)-(-)-1-hexyn-3-ol 
• 70095-35-1 (R)-hex-1-yn-3-yl acetate 
• 105-31-7 (3R)-hex-1-yn-3-ol 
• 1000786-12-8 (S)-(-)-3-acetoxy-1-hexyne 
• 1291103-72-4 N-(R)-(hex-1-yn-3-yl)-N-methylbenzenamine 
• 1432061-32-9 (R)-N-(hex-1-yn-3-yl)-2-methoxybenzenamine 

Relevant academic research and scientific papers

New and efficient synthesis of 1,3-dienylphosphonates by palladium-catalyzed substitution of propargylic esters to diethyl phosphite

An efficient route to the synthesis of 1,3-dienylphosphonates (1) has been developed for the first time by the substitution of propargylic esters (2) to the diethyl phosphite (3) nucleophile in the presence of Pd2 (dba) 3 · CHCl3 (2 mol %) and 2,2′- bis(diphenylphosphino)-1,1′-binaphthyl (4 mol%). Both the alkyl and aryl 1,3-dienylphosphonates can be prepared from this transformation. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.

MILD PROTECTION AND DEPROTECTION OF ALCOHOLS AS TER-BUTYL ETHERS IN THE FIELD OF PHEROMONE SYNTHESIS

α,ο-Halohydrins and ο-acetylenic alcohols are protected as t-butyl ethers by reaction with isobutene and an acid catalyst : Amberlyst H-15. t-Butyl ethers are, in turn, cleaved to acetates by Ac2O and 10 percent FeCl3 in Et2O solvent.Under these mild conditions conjugated dieneic systems are neither destroyed nor isomerized.

Regiospecific Synthesis of a Terminal, Oxyfunctionalized Methyl Ketone Enamines via Catalytic Aminomercuriation of Prop-2-ynyl Esters and Ethers

Catalytic aminomercuriation of 1-substituted prop-2-ynyl esters and ethers (5) provides a mild, simple, and regiospecific route to the terminal functionalized enamines (6) despite the fact that they are potentially isomerisable to their internal form; hyd

Synthesis of optically active alkynyl alcohols and α-hydroxy esters by microbial asymmetric hydrolysis of the corresponding acetates

Asymmetric hydrolysis of the acetates of racemic alkynyl alcohols and α-hydroxy esters by Bacillus subtilis var. Niger afforded optically active acetates and alcohols in 7-90% optical purities. The both enantiomers of optically pure mandelie acid were prepared by this microbial method.