| CAS: | 5332-25-2 |
| MF: | C9H6BrN |
| MW: | 208.05 |
| EINECS: | 226-238-7 |
| Product Categories: | Aromatics;Heterocycles;Quinolines, Isoquinolines & Quinoxalines;Boronic Acid;Heterocyclic Compounds;Building Blocks;Miscellaneous;Quinoline Derivertives;Aromatics Compounds;Haloquinolines;quinoline;Halogenated Heterocycles;Heterocyclic Building Blocks;QuinolinesHeterocyclic Building Blocks;blocks;Bromides;Quinolines;Halides;Quinolines, Isoquinolines & Quinoxalines;Quinoline&Isoquinoline;5332-25-2 |
| Mol File: | 5332-25-2.mol |
 |
|
| 6-Bromoquinoline Chemical Properties |
| Melting point | 19°C |
| Boiling point | 116 °C / 6mmHg |
| density | 1.538 g/mL at 25 °C |
| refractive index | n20/D 1.663 |
| Fp | 19 °C |
| storage temp. | Inert atmosphere,2-8°C |
| solubility | Soluble in acetone, acetonitrile, dichloromethane, ethyl acetate and THF. |
| pka | 4.18±0.10(Predicted) |
| form | Oil |
| color | Thick |
| InChIKey | IFIHYLCUKYCKRH-UHFFFAOYSA-N |
| 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) |
| 6-Bromoquinoline Usage And Synthesis |
| 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 |
| Uses | 6-Bromoquinoline is used as fine chemical and pharmaceutical intermediate, used as the coupling reagent. |
Product picture
Packing &shipping&Payment
Packing:25kg/drum
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
| Quantity(Kilograms) | 1 - 10000 | >10000 |
| Est. Time(days) | 5 | To be negotiated |
Company information
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.
Advantage
In stock
Japan
