3-Bromoquinoline 5332-24-1 manufacturer , better price with good quality
3-Bromoquinoline Basic information |
Product Name: | 3-Bromoquinoline |
Synonyms: | 3-bromo-quinolin;3-BROMOQUINLIINE;3-BROMOQUINOLINE;3-Bromoquinoline98%Or99%;3-Bromoquinoline 98 %;Bromoquinoline;Quinoline, 3-bromo-;3-Bromoquinoline ,98% [HPLC 98%] |
CAS: | 5332-24-1 |
MF: | C9H6BrN |
MW: | 208.05 |
EINECS: | 226-237-1 |
Product Categories: | blocks;Bromides;Quinolines;Halides;Heterocycles;Quinolines, Quinazolines and derivatives;Quinoline&Isoquinoline;Quinoline Derivertives;Aromatics Compounds;Haloquinolines;Aromatics;Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;QuinolinesHeterocyclic Building Blocks |
Mol File: | 5332-24-1.mol |
3-Bromoquinoline Chemical Properties |
mp | 13-15 °C(lit.) |
bp | 274-276 °C(lit.) |
density | 1.533 g/mL at 25 °C(lit.) |
refractive index |
n |
Fp | >230 °F |
storage temp. | Keep Cold |
BRN | 112939 |
CAS DataBase Reference | 5332-24-1(CAS DataBase Reference) |
NIST Chemistry Reference | Quinoline, 3-bromo-(5332-24-1) |
EPA Substance Registry System | Quinoline, 3-bromo-(5332-24-1) |
Safety Information |
Hazard Codes | Xi |
Risk Statements | 36/37/38 |
Safety Statements | 26-36-37/39 |
WGK Germany | 3 |
MSDS Information |
Provider | Language |
---|---|
3-Bromoquinoline | English |
ACROS | English |
SigmaAldrich | English |
ALFA | English |
3-Bromoquinoline Usage And Synthesis |
Bromoquinoline |
There are seven position isomers with the main properties are as follows:
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Application and synthesis method |
3-Bromoquinoline can have action with mixed acid to generate 3-bromo-5-nitroquinoline, followed by heating with potassium permanganate to be oxidized to 5-bromo-2, 3-pyridine dicarboxylic acid. 6-bromo-quinoline can be heated together nitric acid to generate 6-bromo-8-nitro-quinoline, followed by reaction with potassium permanganate to be oxidized into 2, 3-pyridinedicarboxylic acid. 2-bromo-quinoline can be manufactured through the reaction between 2-hydroxyquinoline and phosphorus pentabromide 3-bromo-quinoline can be obtained through heating the quinoline perbromide at 180 ° C. 4-bromoquinoline can be obtained through either the heating reaction between 4-hydroxyquinoline and phosphorus pentabromide or by the diazotization reaction of 4-aminoquinoline. 5-bromo-quinoline can be obtained from the heating reaction between m-bromo aniline, glycerol, m-bromonitrobenzene and concentrated sulfuric acid, or through the diazotization reaction of 5-amino-quinoline. 6-bromo-quinoline can be obtained through the heating reaction between p-bromoaniline, glycerol, concentrated sulfuric acid and p-bromo-nitrobenzene. 7-bromoquinoline can be obtained through the diazotization of 7-aminoquinoline. 8-bromo-quinoline can be obtained through the heating of o-bromo aniline, glycerol, concentrated sulfuric acid and o-bromo-nitrobenzene in the heating system. Purposes: as organic synthesis reagents. |
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Uses |
For pharmaceuticals Medicine, pesticide intermediates |
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Chemical Properties | colorless to light yellow liquid |
3-Bromoquinoline Preparation Products And Raw materials |
Preparation Products | 5-Aminonicotinic acid-->3-Quinolinecarboxaldehyde-->3-Quinolineboronic acid-->3-Aminoquinoline-->3-BROMOQUINOLINE-8-SULFONIC ACID |
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