ChemicalBook--->CAS DataBase List--->7496-46-0

7496-46-0

7496-46-0 Structure

7496-46-0 Structure
IdentificationBack Directory
[Name]

8-Bromomethylquinoline
[CAS]

7496-46-0
[Synonyms]

8-(BROMOMETHYL)QUINOLINE
8-QuinolylMethyl broMide
8-Quinolinylmethyl bromide
Quinoline, 8-(bromomethyl)-
8-(Bromomethyl)quinoline ,97%
8-(Bromomethyl)-1-azanaphthalene
8-(Bromomethyl)quinoline >=96.5% (GC)
8-Bromomethylquinoline ISO 9001:2015 REACH
[Molecular Formula]

C10H8BrN
[MDL Number]

MFCD00047621
[MOL File]

7496-46-0.mol
[Molecular Weight]

222.08
Questions And AnswerBack Directory
[Uses]

8-Bromomethylquinoline is an intermediate in synthesizing 8-Quinolinemethanamine Dihydrochloride (Q700700), which is a salt form of 8-Quinolinemethanamine. 8-Quinolinemethanamine is used in the preparation of quinazolinone derivatives as anti-tumor agents.
Chemical PropertiesBack Directory
[Melting point ]

81 °C
[Boiling point ]

321.9±17.0 °C(Predicted)
[density ]

1.518±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Dichloromethane
[form ]

Solid
[pka]

3.85±0.17(Predicted)
[color ]

White
[BRN ]

119140
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H318
[Precautionary statements ]

P280-P301+P312+P330-P305+P351+P338+P310
[Hazard Codes ]

C,Xn
[Risk Statements ]

34-22-52-41
[Safety Statements ]

26-36/37/39-45-24/25-22-39
[RIDADR ]

3261
[WGK Germany ]

3
[Hazard Note ]

Corrosive
[HazardClass ]

IRRITANT
[HS Code ]

29334900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sodium hydroxide-->Ethyl acetate-->Sulfuric acid-->Petroleum ether-->Sodium sulfate-->Sodium chloride-->Carbon tetrachloride-->N-Bromosuccinimide-->Benzoyl peroxide-->Glycerol-->o-Toluidine-->Sodium iodide-->PROPANENTRILE,2,2'-[(1E)-1,2-DIAZENEDIYL]BIS(2-METHYLPROPIONITRILE)-->3-Bromo-8-(bromomethyl)quinoline-->5-bromo-8-(bromomethyl)quinoline-->8-(Dibromomethyl)quinoline ,99.5%-->8-Methylquinoline
Hazard InformationBack Directory
[Chemical Properties]

Light yellow powder
[Synthesis]

8-Methylquinoline

611-32-5

8-Bromomethylquinoline

7496-46-0

To a pre-dried 300 mL three-necked flask under nitrogen atmosphere were added 8-methylquinoline (10.0 g, 69.8 mmol), benzoyl peroxide (0.843 g, 3.49 mmol) and cyclohexane (150 mL). Under stirring conditions, N-bromosuccinimide (13.6 g, 76.8 mmol) was added in batches. The reaction mixture was refluxed for 10 hours. After completion of the reaction, the reaction mixture was filtered. The filtrate was washed sequentially with saturated aqueous sodium bicarbonate (3 x 100 mL) and brine (100 mL) and then dried with anhydrous sodium sulfate. Subsequently, the solvent was removed by vacuum evaporation. Finally, recrystallization was carried out using ether and hexane to give the light brown solid product 8-bromomethylquinoline (7.1 g, 46% yield).

[References]

[1] Journal of Heterocyclic Chemistry, 2001, vol. 38, # 1, p. 1 - 9
[2] Journal of Organometallic Chemistry, 1994, vol. 484, # 1-2, p. C8 - C9
[3] Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1995, # 13, p. 2289 - 2296
[4] Chemical and Pharmaceutical Bulletin, 2000, vol. 48, # 4, p. 477 - 479
[5] Chemical and Pharmaceutical Bulletin, 1989, vol. 37, # 8, p. 2109 - 2116
Spectrum DetailBack Directory
[Spectrum Detail]

8-Bromomethylquinoline(7496-46-0)1HNMR
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