ChemicalBook > CAS DataBase List > 6-bromo-7-methylquinoline

6-bromo-7-methylquinoline

Product Name
6-bromo-7-methylquinoline
CAS No.
122759-89-1
Chemical Name
6-bromo-7-methylquinoline
Synonyms
6-bromo-7-methylquinoline;Quinoline, 6-bromo-7-methyl-
CBNumber
CB82537630
Molecular Formula
C10H8BrN
Formula Weight
222.08
MOL File
122759-89-1.mol
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6-bromo-7-methylquinoline Property

Density 
1.488
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to light brown Solid
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Safety

HS Code 
2933499090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H317May cause an allergic skin reaction

H318Causes serious eye damage

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

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N-Bromosuccinimide Price

TRC
Product number
B697695
Product name
6-Bromo-7-methylquinoline
Packaging
100mg
Price
$45
Updated
2021/12/16
TRC
Product number
B697695
Product name
6-Bromo-7-methylquinoline
Packaging
250mg
Price
$85
Updated
2021/12/16
ChemScene
Product number
CS-W007221
Product name
6-Bromo-7-methylquinoline
Packaging
1g
Price
$63
Updated
2021/12/16
Apolloscientific
Product number
OR43652
Product name
6-Bromo-7-methylquinoline
Packaging
1g
Price
$240
Updated
2021/12/16
SynQuest Laboratories
Product number
3H32-9-5J
Product name
6-Bromo-7-methylquinoline
Packaging
1g
Price
$264
Updated
2021/12/16
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6-bromo-7-methylquinoline Chemical Properties,Usage,Production

Chemical Properties

Yellow solid

Synthesis

6933-10-4

56-81-5

122759-89-1

General procedure for the synthesis of 6-bromo-7-methylquinoline from 4-bromo-3-methylaniline and glycerol: [0304] A mixture of 4-bromo-3-methylaniline (20 g, 107.5 mmol), ferric sulfate (6.6 g, 43.4 mmol), glycerol (40.8 g, 440 mmol) and nitrobenzene (8.12 g, 66 mmol) was mixed with concentrated sulfuric acid (23 ml) and slowly heated. After the initial vigorous reaction subsided, the reaction mixture was refluxed for 3 h. The excess nitrobenzene was subsequently removed by evaporation. The pH was adjusted to 7-8 by adding saturated aqueous sodium bicarbonate solution to the reaction mixture and then filtered. The filtrate was extracted with dichloromethane and the organic layers were combined and dried over anhydrous sodium sulfate. The dried organic phase was filtered and concentrated in vacuum and the resulting solid was purified by fast column chromatography. The purified yellow solid was further washed with petroleum ether to afford 7.5 g of 6-bromo-7-methylquinoline in 31% yield. The structure of the product was confirmed by 1H NMR (CDCl3): δ 2.60 (s, 3H), 7.36 (m, 1H), 7.96 (s, 1H), 8.04 (m, 2H), 8.89 (m, 1H).

References

[1] Patent: WO2008/51808, 2008, A2. Location in patent: Page/Page column 79-80

6-bromo-7-methylquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

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6-bromo-7-methylquinoline Suppliers

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122759-89-1, 6-bromo-7-methylquinolineRelated Search:


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