26323-01-3

Basic information

• Product Name: Quinolinium,1-(phenylmethyl)-, bromide (1:1)
• Synonyms: 1-Benzylquinoliniumbromide (7CI); Quinolinium, 1-(phenylmethyl)-, bromide (9CI); Quinolinium,1-benzyl-, bromide (8CI); Benzylquinolinium bromide
• CAS NO: 26323-01-3
• Molecular Formula: Br*C₁₆H₁₄N
• Molecular Weight: 220.2885
• Mol File: 26323-01-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• CAS DataBase Reference: Quinolinium,1-(phenylmethyl)-, bromide (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: Quinolinium,1-(phenylmethyl)-, bromide (1:1)(26323-01-3)
• EPA Substance Registry System: Quinolinium,1-(phenylmethyl)-, bromide (1:1)(26323-01-3)

Safety Data

• Hazardous Substances Data: 26323-01-3(Hazardous Substances Data)

Upstream product

• 91-22-5 quinoline 
• 100-39-0 benzyl bromide 
• 536-74-3 phenylacetylene 

Downstream Products

• 959628-38-7 1-benzyl-2-(tribromomethyl)-1,2-dihydroquinoline 

Relevant articles and documents

A quinolinium-derived turn-off fluorescent anion sensor

A quinolinium-derived anion sensor has been synthesised which shows a turn-off fluorescence response in the presence of anions, with selectivity for acetate. The compound exhibits complex anion binding comprising of a host dimer, 2:1 and 1:1 host:guest sp

N-substituted 1,2-dihydroquinolines as anticancer agents: Electronic control of redox stability, assessment of antiproliferative effects, and mechanistic insights

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Copper-Catalyzed Selective 1,2-Difunctionalization of N-Heteroaromatics through Cascade C-N/CC/CO Bond Formation

This study presents an efficient strategy for constructing 1,2-difunctionalized quinoline derivatives via the multicomponent cascade coupling of N-heteroaromatics with alkyl halides and different terminal alkynes. This reaction was achieved through sequential functionalization at the one- and two-positions of quinolines, which displayed a broad substrate scope, environmental friendliness, excellent functional group tolerance, high atom efficiency, and chemoselectivity. The multicomponent coupling involved the abnormal construction of new C-N, CC, and CO bonds in one pot. The applicability of this method was further demonstrated by the late-stage functionalization of complex drug molecules under the established conditions.

Arylamine derivative synthesized by deconstructing aza-aromatic hydrocarbon as well as method and application thereof

The invention belongs to the technical field of pharmaceutical chemicals, and discloses an arylamine derivative synthesized by deconstructing an aza-aromatic hydrocarbon as well as a method and application thereof. The method comprises the following steps