3-Quinolinecarboxaldehyde, 6-broMo-

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3-Quinolinecarboxaldehyde, 6-broMo- manufacturers

3-Quinolinecarboxaldehyde, 6-broMo- Basic information
Product Name:3-Quinolinecarboxaldehyde, 6-broMo-
Synonyms:3-Quinolinecarboxaldehyde, 6-broMo-;6-broMo-3-Quinolinecarboxaldehyde
CAS:1196155-68-6
MF:C10H6BrNO
MW:236.06
EINECS:
Product Categories:
Mol File:1196155-68-6.mol
3-Quinolinecarboxaldehyde, 6-broMo- Structure
3-Quinolinecarboxaldehyde, 6-broMo- Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceLight yellow to green yellow Solid
InChIInChI=1S/C10H6BrNO/c11-9-1-2-10-8(4-9)3-7(6-13)5-12-10/h1-6H
InChIKeyPCHCYMZZDAUVQB-UHFFFAOYSA-N
SMILESN1C2C(=CC(Br)=CC=2)C=C(C=O)C=1
Safety Information
MSDS Information
3-Quinolinecarboxaldehyde, 6-broMo- Usage And Synthesis
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
3-Quinolinecarboxaldehyde, 6-broMo- Preparation Products And Raw materials
Raw materials(6-BroMoquinolin-3-yl)Methanol-->Dichloromethane-->Manganese dioxide
Tag:3-Quinolinecarboxaldehyde, 6-broMo-(1196155-68-6) Related Product Information
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