103854-56-4

Basic information

• Product Name: Ketone, methyl 5-quinolyl (6CI)
• Synonyms: Ketone, methyl 5-quinolyl (6CI);1-Quinolin-5-ylethanone;CAS:103854-56-4;Ethanone,1-(5-quinolinyl)-
• CAS NO: 103854-56-4
• Molecular Formula: C₁₁H₉NO
• Molecular Weight: 171.198
• Product Categories: ACETYLGROUP
• Mol File: 103854-56-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 315.207°C at 760 mmHg
• Flash Point: 152.423°C
• Appearance: /
• Density: 1.154g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: Ketone, methyl 5-quinolyl (6CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ketone, methyl 5-quinolyl (6CI)(103854-56-4)
• EPA Substance Registry System: Ketone, methyl 5-quinolyl (6CI)(103854-56-4)

Safety Data

• Hazardous Substances Data: 103854-56-4(Hazardous Substances Data)

Usage

General Description

Ketone, methyl 5-quinolyl is a chemical compound with the molecular formula C11H9NO. It is a ketone derivative of 5-quinolyl, and its systematic name is 4-oxo-2-methyl-3H-quinoline. Ketone, methyl 5-quinolyl (6CI) is commonly used as a precursor in the synthesis of pharmaceuticals and agrochemicals. It is a colorless to pale yellow liquid with a characteristic odour and is soluble in organic solvents. Ketone, methyl 5-quinolyl is known to have potential applications in the fields of medicine, agriculture, and chemical research due to its versatile chemical properties.

InChI:InChI=1/C11H9NO/c1-8(13)9-4-2-6-11-10(9)5-3-7-12-11/h2-7H,1H3

Upstream product

• 111-34-2 -butyl vinyl ether 
• 177734-78-0 5-trifluoromethanesulphonyloxyquinoline 
• 22934-41-4 quinoline-5-carbaldehyde 
• 880782-86-5 1-(quinolin-5-yl)ethan-1-ol 
• 99-03-6 1-(3-aminophenyl)ethanone 
• 56-81-5 glycerol 
• 4964-71-0 5-bromoquinoline 
• 97674-02-7 tributyl(1-ethoxyvinyl)stannane 

Downstream Products

• 880782-86-5 1-(quinolin-5-yl)ethan-1-ol 

Relevant articles and documents

Quinoline and phenanthroline preparation starting from glycerol via improved microwave-assisted modified Skraup reaction

An efficient "green" modified Skraup reaction in neat water was developed using inexpensive, abundant and environmentally-friendly glycerol under microwave irradiation conditions. Starting from aniline derivatives, various quinolines were obtained in 10-66% yields. The use of nitroaniline led to the corresponding phenanthrolines in 15-52% yields, respectively. This journal is the Partner Organisations 2014.

10A-AZALIDE COMPOUND HAVING 4-MEMBERED RING STRUCTURE

A 10a-azalide compound having a 4-membered ring structure crosslinked at the 10a- and 12-positions, which is represented by the formula (I), and is effective on even Haemophilus influenzae, or erythromycin resistant bacteria (e.g., resistant pneumococci and streptococci).

CALCIUM RECEPTOR MODULATING ARYLALKYLAMINES

The compounds of the invention are represented by the following general structure (I) or a pharmaceutically acceptable salt thereof, and compositions containing them, wherein the variables are defined herein, and their use to reduce or inhibit PTH secretion, including methods for reducing or inhibiting PTH secretion and methods for treatment or prophylaxis of diseases associated with bone disorders, such as osteoporosis, or associated with excessive secretion of PTH, such as hyperparathyroidism. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.