10522-43-7

Basic information

• Product Name: CHEMBRDG-BB 5175124
• Synonyms: CHEMBRDG-BB 5175124;2,5-DIMETHYL-8-QUINOLINOL;2,5-dimethyl-8-quinolinol(SALTDATA: FREE);2,5-Dimethylquinolin-8-ol
• CAS NO: 10522-43-7
• Molecular Formula: C11H11NO
• Molecular Weight: 173.22
• Mol File: 10522-43-7.mol

Chemical Properties

• Boiling Point: 321.6°C at 760 mmHg
• Flash Point: 148.3°C
• Appearance: /
• Density: 1.172g/cm³
• Vapor Pressure: 0.000157mmHg at 25°C
• Refractive Index: 1.647
• CAS DataBase Reference: CHEMBRDG-BB 5175124(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 5175124(10522-43-7)
• EPA Substance Registry System: CHEMBRDG-BB 5175124(10522-43-7)

Safety Data

• Hazardous Substances Data: 10522-43-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H11NO/c1-7-3-6-10(13)11-9(7)5-4-8(2)12-11/h3-6,13H,1-2H3

Upstream product

• 123-73-9 trans-Crotonaldehyde 
• 95-84-1 3-amino-4-hydroxytoluene 
• 64-17-5 ethanol 
• 123-72-8 butyraldehyde 

Relevant articles and documents

Synthesis, spectroscopy and computational studies of selected hydroxyquinolines and their analogues

Synthetic, spectroscopy and mechanistic aspects of preparation of selected hydroxyquinolines and their analogues or derivatives contained methoxy, fluoro, chloro, carboxylic, carbodithioic and phosphinate or dioxaphosphinane groups were elaborated. The mu

Study on Relationship Between Fluorescence Properties and Structure of Substituted 8-Hydroxyquinoline Zinc Complexes

Organic light-emitting diodes (OLEDs) produced from 8-hydroxyquinoline metal complexes play a vital role in modern electroluminescent devices. In this manuscript, a series of 8-hydroxyquinoline derivatives were synthesized by different methods and their corresponding zinc metal complexes were prepared. The UV and fluorescence properties of the complexes were measured aiming to understand the effect of substituents at the quinoline ring on the fluorescence properties of the complexes. When the C-5 of 8-hydroxyquinoline was replaced by halogen group, the fluorescence emission wavelengths had been red-shifted, at the same time, blue-shifted of fluorescence emission wavelength was observed when the C-5 position of 8-hydroxyquinoline was substituted by electron-withdrawing group. When the C-4 position of 8-hydroxyquinolie was substituted by methyl or the C-5 position was substituted by sulfonic acid group, the corresponding zinc complexes had higher fluorescence intensity than 8-hydroxyquinolie zinc.

Assembly of Diversely Substituted Quinolines via Aerobic Oxidative Aromatization from Simple Alcohols and Anilines

An aerobic oxidative aromatization of simple aliphatic alcohols and anilines under the Pd(OAc)2/2,4,6-Collidine/Br?nsted acid catalytic system has been established, providing a direct approach for the preparation of diverse substituted quinoline derivatives in high yields with wide functional group tolerance. Practically, the protocol can be easily scaled up to gram-scale and was utilized in the concise formal synthesis of a promising herbicide candidate.