6-Bromoquinoline

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1 Kilogram	Negotiable

1 Kilogram

Negotiable

Min.Order :1 Kilogram
Purity: 98%
Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

6-Bromoquinoline 5332-25-2 C9H6BrN

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Appearance:powder
Application:5332-25-2
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ProductionCapacity:300|Kilogram|Month
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Product Name:	6-Bromoquinoline
Synonyms:	6-BROMOQUINOLINE;TIMTEC-BB SBB001559;6-bromo-quinolin;Quinoline, 6-bromo-;6-BROMOQUINOLINE 95+%;6-BROMOOQUINOLINE;6-Bromoquinoline ,98%;NSC 3996
CAS:	5332-25-2
MF:	C9H6BrN
MW:	208.05
EINECS:	206-363-3
Product Categories:	blocks;Bromides;Quinolines;Halides;Quinolines, Isoquinolines & Quinoxalines;Quinoline&Isoquinoline;Miscellaneous;Quinoline Derivertives;Aromatics Compounds;Haloquinolines;quinoline;Aromatics;Heterocycles;Quinolines, Isoquinolines & Quinoxalines;Boronic Acid;Heterocyclic Compounds;Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;QuinolinesHeterocyclic Building Blocks
Mol File:	5332-25-2.mol

Melting point	19°C
Boiling point	116 °C / 6mmHg
density	1.55
refractive index	n20/D 1.663
Fp	19 °C
storage temp.	Refrigerator
CAS DataBase Reference	5332-25-2(CAS DataBase Reference)
NIST Chemistry Reference	6-Bromo quinoline(5332-25-2)
EPA Substance Registry System	Quinoline, 6-bromo-(5332-25-2)

Hazard Codes	Xi,Xn
Risk Statements	36/37/38-41-37/38-22-20/21/22
Safety Statements	26-37/39-39-36
Hazard Note	Irritant
HazardClass	IRRITANT

Bromoquinoline	There are seven positional isomers of bromoquinoline and their main properties are listed below:
Application and synthetic method	3-bromo-quinoline is reacted with mixed acid for generating 3-bromo-5-nitro-quinoline, which heats together with potassium permanganate for being oxidation into 5-bromo-2, 3-pyridine dicarboxylic acid. 6-bromo-quinoline is heated together with nitric acid to generate 6-bromo-8-nitro quinolone with further reaction with potassium permanganate for being oxidized to 2, 3-pyridinedicarboxylic acid. 2-bromo-quinolien can be synthesized through the reaction between 2-hydroxy quinoline and phosphorus pentabromide. Quinoline perbromide is heated at 180 °C for generating 3-bromo-quinoline. From the heating between 4-hydroxy quinoline and phosphorus pentabromide, or from the diazotization reaction via 4-aminoquinoline to generate 4-bromo-quinoline; 5-bromo-quinoline is synthesize by the heating reaction between m-bromo-aniline, glycerol, m-bromo nitrobenzene and concentrated sulfuric acid, or from the diazotization reaction of 5-aminoquinoline. 6-bromo-quinoline can be synthesized from the heating of bromoaniline, glycerol, concentrated sulfuric acid, and p-bromo-nitrobenzene. 7-bromo-quinoline can be synthesized from the diazotization reaction of 7-aminoquinoline. 8-bromo-quinoline can be synthesized from the heating reaction of o-bromo-aniline, glycerol, concentrated sulfuric acid and o-bromo nitrobenzene. application: as organic synthesis reagents. The above information is edited by the Chemicalbook of Dai Xiongfeng.
Chemical Properties	Thick Oil

6-Bromoquinoline