• Product Name8-Bromomethylquinoline
  • CasNo. 7496-46-0
  • MFC10H8BrN
  • MW222.084
  • Purity
  • Appearance
  • Packing
  • Contact usInquiry

Product Details

CasNo: 7496-46-0

MF: C10H8BrN

Quality Factory Hot Selling 8-Bromomethylquinoline 7496-46-0 with Fast Shipping

  • Molecular Formula:C10H8BrN
  • Molecular Weight:222.084
  • Vapor Pressure:0.000544mmHg at 25°C 
  • Melting Point:81-82 °C 
  • Refractive Index:1.673 
  • Boiling Point:321.9 °C at 760 mmHg 
  • PKA:3.85±0.17(Predicted) 
  • Flash Point:148.5 °C 
  • PSA:12.89000 
  • Density:1.518 g/cm3 
  • LogP:3.12970 

8-Bromomethylquinoline(Cas 7496-46-0) Usage

InChI:InChI=1/C10H8BrN/c11-7-9-4-1-3-8-5-2-6-12-10(8)9/h1-6H,7H2

7496-46-0 Relevant articles

Alkaloids from plants of the Nitraria genus. structure of sibiridine

Tulyaganov,Allaberdiev

, p. 292 - 293 (2003)

The new alkaloid sibiridine was isolated...

A new diaza-18-crown-6 ligand containing two quinolin-8-ylmethyl side arms: Crystal structures and characterization of the ligand, the protonated ligand and its mononuclear Barium(II) and dinuclear copper(II) complexes

Dalley,Xue,Bradshaw,Xian Xin Zhang,Harrison,Savage,Krakowiak,Izatt

, p. 1 - 9 (2001)

A new 7,16-bis(quinolin-8-ylmethyl)-1,4,...

New 1,4,7,10-Tetraazacyclotridecane-11,13-dione Ligands appended with Additional Donor(s) 8-Methylquinoline(s): Crystal Structures and Characterization of their Copper(II) Complexes

Bu, Xian He,An, Dao Li,Chen, Yun Ti,Shionoya, Mitsuhiko,Kimura, Eiichi

, p. 2289 - 2296 (1995)

Two macrocyclic dioxotetraamine ligands ...

Effect of the linking position of a side chain in bis(quinolylmethyl)ethylenediamine as a DNA binding agent

Mikata, Yuji,Onchi, Yoko,Kishigami, Maki,Yano, Shigenobu

, p. 477 - 479 (2000)

Two bisquinoline derivatives, N,N'-bis(2...

THERAPEUTIC COMPOUNDS AND METHODS TO TREAT INFECTION

-

Paragraph 0468-0469, (2019/02/13)

Disclosed herein are compounds of formul...

Metal-Free Oxidative B?N Coupling of nido-Carborane with N-Heterocycles

Yang, Zhongming,Zhao, Weijia,Liu, Wei,Wei, Xing,Chen, Meng,Zhang, Xiao,Zhang, Xiaolei,Liang, Yong,Lu, Changsheng,Yan, Hong

supporting information, p. 11886 - 11892 (2019/07/18)

A general method for the oxidative subst...

A general method for the metal-free, regioselective, remote C-H halogenation of 8-substituted quinolines

Motati, Damoder Reddy,Uredi, Dilipkumar,Watkins, E. Blake

, p. 1782 - 1788 (2018/02/23)

An operationally simple and metal-free p...

Unprecedented Reaction Pathway of Sterically Crowded Calcium Complexes: Sequential C?N Bond Cleavage Reactions Induced by C?H Bond Activations

Yang, Yang,Wang, Haobing,Ma, Haiyan

supporting information, p. 239 - 247 (2017/02/05)

Five bis(quinolylmethyl)-(1H-indolylmeth...

7496-46-0 Process route

8-methylquinoline
611-32-5

8-methylquinoline

8-bromomethyl-quinoline
7496-46-0

8-bromomethyl-quinoline

Conditions
Conditions Yield
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 12h; Heating;
88%
With N-Bromosuccinimide; Perbenzoic acid; In tetrachloromethane; for 6h; Heating;
85%
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 3h; Reflux;
82%
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 36h; Heating;
80%
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 2h;
75%
With N-Bromosuccinimide; Perbenzoic acid; In tetrachloromethane; for 3h; Heating;
58%
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 6h; Reflux; Inert atmosphere;
58%
With N-Bromosuccinimide; dibenzoyl peroxide; In cyclohexane; for 10h; Inert atmosphere; Reflux;
46%
With tetrachloromethane; N-Bromosuccinimide; dibenzoyl peroxide; Irradiation.mit UV-Licht;
With N-Bromosuccinimide;
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; Heating;
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 6h; Heating;
With N-Bromosuccinimide; In tetrachloromethane; at 60 ℃; for 1h;
0.5 g
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; chloroform;
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane;
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane;
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; water; Heating / reflux;
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In 1,2-dichloro-ethane; for 30h; Reflux; Inert atmosphere;
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; Heating / reflux;
With N-Bromosuccinimide; In tetrachloromethane; Inert atmosphere; Schlenk technique; Reflux;
8-methylquinoline
611-32-5

8-methylquinoline

azobisisobutyronitrile
34241-39-9

azobisisobutyronitrile

8-bromomethyl-quinoline
7496-46-0

8-bromomethyl-quinoline

Conditions
Conditions Yield
With N-Bromosuccinimide; In tetrachloromethane;

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