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866831-75-6

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866831-75-6 Usage

General Description

2-Bromoquinoline-4-carboxaldehyde is a chemical compound with the molecular formula C10H6BrNO. It is a yellow to orange solid with a molecular weight of 237.07 g/mol. 2-Bromoquinoline-4-carboxaldehyde is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also used as a reagent in organic synthesis and as a fluorescent labeling reagent for detection of biological molecules. 2-Bromoquinoline-4-carboxaldehyde is classified as a hazardous substance and should be handled with caution, as it may cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 866831-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,8,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 866831-75:
(8*8)+(7*6)+(6*6)+(5*8)+(4*3)+(3*1)+(2*7)+(1*5)=216
216 % 10 = 6
So 866831-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H6BrNO/c11-10-5-7(6-13)8-3-1-2-4-9(8)12-10/h1-6H

866831-75-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoquinoline-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-Quinolinecarboxaldehyde,2-bromo

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:866831-75-6 SDS

866831-75-6Downstream Products

866831-75-6Relevant articles and documents

Regioselective lithium-halogen exchange and palladium-catalyzed cross-coupling reactions of 2,4-dihaloquinolines

Comins, Daniel L.,Nolan, Jason M.,Bori, Ibrahim D.

, p. 6697 - 6699 (2005)

Lithium-halogen exchange of 2,4-dibromoquinolines proceeds regioselectively at C-4 and affords 4-substituted quinolines on quenching with electrophiles. Palladium-catalyzed cross-coupling reactions of 2-bromo-4-iodoquinoline provide 4-substituted 2-bromoq

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