824430-39-9

Basic information

• Product Name: 1-Naphthalenecarbonyl chloride, 4-ethyl-
• Synonyms: 4-ethyl-1-naphthoyl chloride;1-Naphthalenecarbonyl chloride,4-ethyl
• CAS NO: 824430-39-9
• Molecular Formula: C13H11ClO
• Molecular Weight: 218.683
• Mol File: 824430-39-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenecarbonyl chloride, 4-ethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenecarbonyl chloride, 4-ethyl-(824430-39-9)
• EPA Substance Registry System: 1-Naphthalenecarbonyl chloride, 4-ethyl-(824430-39-9)

Safety Data

• Hazardous Substances Data: 824430-39-9(Hazardous Substances Data)

Usage

General Description

1-Naphthalenecarbonyl chloride, 4-ethyl- is a chemical compound with the molecular formula C14H11ClO. It is a derivative of naphthalene and has a carbonyl chloride functional group with an ethyl substituent. 1-Naphthalenecarbonyl chloride, 4-ethyl- is commonly used as a reagent in organic synthesis for the introduction of the 1-naphthoyl group into other compounds. It can also be used in the preparation of various pharmaceuticals and agrochemicals. Additionally, it has applications in the manufacturing of dyes and pigments, as well as in the production of other organic chemicals.

Upstream product

• 1127-76-0 1-ethylnapthelene 
• 824430-38-8 N,N-diphenyl-4-ethyl-1-naphthalenecarboxamide 
• 91902-58-8 4-ethyl-1-naphthalenecarboxylic acid 

Downstream Products

• 824959-83-3 JWH-213 
• 824959-81-1 JWH-210 

Relevant articles and documents

Synthesis and characterization of 3-aminoquinoline derivatives and studies of photophysicochemical behaviour and antimicrobial activities

A series of 3-aminoquinoline derivatives were synthesized, where their chemical structures were confirmed by various analytical techniques, such as, Elemental Analysis, Nuclear Magnetic Resonance Spectroscopy (1H and 13C NMR), Liquid Chromatography-Mass-Mass Spectroscopy (LC-MS-MS), Ultraviolet-Visible Spectroscopy (UV-Vis), Fourier Transform Infrared Spectroscopy (FTIR) and Photoluminescence (PL). The quinoline ring core, typical of aminoquinolines, and a naphthalene group was combined to devise (4-alkyl-1-naphthyl)-quinolin-3-ylamide derivatives. These derivatives were designed and synthesized in light of the chemical and biological profiles of these important subunits. All the compounds were evaluated for their in vitro antibacterial and antifungal activities by the paper disc diffusion method with Gram-positive Bacillus subtilis, Bacillus megaterium and Staphylococcus aureus, Gram-negative Enterobacter aerogenes, Eschericha coli, Klebsiella pneumoniae and Pseudomonas aeruginosa and yeasts Candida albicans, Saccharomyces cerevisiae and Yarrovia lipolytica. These compounds showed antimicrobial activities against Gram-positive and Gram-negative bacteria and several yeasts, and thus their activity was not restricted to any particular type of microorganism.

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