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Quinolin-8-yl chloroacetate is an organic compound with the chemical formula C12H8ClNO2. It is a derivative of quinoline, a heterocyclic aromatic compound, and chloroacetic acid. quinolin-8-yl chloroacetate is characterized by the presence of a quinoline ring system, which is fused to a pyridine ring, and a chloroacetyl group attached to the 8-position of the quinoline. Quinolin-8-yl chloroacetate is a white crystalline solid and is soluble in organic solvents. It is used as a synthetic intermediate in the preparation of various pharmaceuticals and agrochemicals, particularly those involving the quinoline moiety. Due to its reactivity, it is important to handle quinolin-8-yl chloroacetate with care, following appropriate safety protocols.

5568-49-0

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5568-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5568-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5568-49:
(6*5)+(5*5)+(4*6)+(3*8)+(2*4)+(1*9)=120
120 % 10 = 0
So 5568-49-0 is a valid CAS Registry Number.

5568-49-0SDS

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 quinolin-8-yl 2-chloroacetate

1.2 Other means of identification

Product number -
Other names 8-Chloracetoxy-chinolin

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:5568-49-0 SDS

5568-49-0Relevant academic research and scientific papers

SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF CERTAIN QUINOLINE DERIVATIVES

Adb-Alla, Mohamed A.,Ahmed, Abdel-Hamid N.,El-Zohry, Maher F.,Omar, Farghaly A.

, p. 1547 - 1552 (2007/10/02)

Some aryl or heterocyclic mercaptans reacted with 8-quinolyl chloroacetate II or 8-quinolinoxyacetyl chloride IV to give the corresponding 8-quinolyl-α-mercaptoacetate V or 8-quinolyloxy thioacetate VI, respectively.The mercaptans V were oxidized to the corresponding sulfones VII.Some of these compounds were tested for their antimicrobial activities in comparison with tetracycline reference compound.

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