ChemicalBook--->CAS DataBase List--->1196155-68-6

1196155-68-6

1196155-68-6 Structure

1196155-68-6 Structure
IdentificationBack Directory
[Name]

3-Quinolinecarboxaldehyde, 6-broMo-
[CAS]

1196155-68-6
[Synonyms]

6-broMo-3-Quinolinecarboxaldehyde
3-Quinolinecarboxaldehyde, 6-broMo-
[Molecular Formula]

C10H6BrNO
[MDL Number]

MFCD13190233
[MOL File]

1196155-68-6.mol
[Molecular Weight]

236.06
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
[Appearance]

Light yellow to green yellow Solid
[InChI]

InChI=1S/C10H6BrNO/c11-9-1-2-10-8(4-9)3-7(6-13)5-12-10/h1-6H
[InChIKey]

PCHCYMZZDAUVQB-UHFFFAOYSA-N
[SMILES]

N1C2C(=CC(Br)=CC=2)C=C(C=O)C=1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

3-Quinolinecarboxaldehyde, 6-broMo-(1196155-68-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

(6-BroMoquinolin-3-yl)Methanol

1345445-92-2

3-Quinolinecarboxaldehyde, 6-broMo-

1196155-68-6

General procedure for the synthesis of 6-bromoquinoline-3-carbaldehyde from (6-bromoquinolin-3-yl)methanol: (6-bromoquinolin-3-yl)methanol (716 mg, 2.70 mmol) was dissolved in dichloromethane (9 mL), manganese dioxide (705 mg, 8.12 mmol) was added, and the reaction was stirred at 20°C for 2 days. After completion of the reaction, the mixture was filtered through diatomaceous earth and the filtrate was concentrated under reduced pressure to afford the target product 6-bromoquinoline-3-carbaldehyde (577 mg, 63% yield).

[References]

[1] Patent: WO2011/131741, 2011, A1. Location in patent: Page/Page column 92
[2] Patent: US2012/94976, 2012, A1. Location in patent: Page/Page column 58
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