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6-Chloromethylquinoline, a member of the quinolines family, is a heterocyclic compound with the chemical formula C10H8ClN. It is not found naturally and is synthesized in laboratories. 6-CHLOROMETHYLQUINOLINE is known for its reactivity and versatility, making it a valuable component in chemical synthesis, particularly for the production of pharmaceutical drugs. Due to its potential environmental impact and health risks, it should be handled with caution.

2644-82-8

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2644-82-8 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloromethylquinoline is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its bioactive properties and reactivity make it a valuable component in the development of new medications.
Used in Chemical Synthesis:
6-Chloromethylquinoline is used as a building block in the synthesis of complex organic compounds. Its versatility allows for the creation of a wide range of chemical products, contributing to the advancement of the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 2644-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2644-82:
(6*2)+(5*6)+(4*4)+(3*4)+(2*8)+(1*2)=88
88 % 10 = 8
So 2644-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H8ClN/c11-7-8-3-4-10-9(6-8)2-1-5-12-10/h1-6H,7H2

2644-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(chloromethyl)quinoline

1.2 Other means of identification

Product number -
Other names Quinoline,6-(chloromethyl)

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:2644-82-8 SDS

2644-82-8Relevant academic research and scientific papers

PYRROLIDINE GLYCOSIDASE INHIBITORS

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Page/Page column 139, (2020/03/15)

Compounds of formula (I) wherein A, W, R3b, Z and p have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

MALONONITRILE OXIME ETHER COMPOUND AND USE THEREOF

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Paragraph 0115; 0116, (2019/01/04)

Disclosed is a malononitrile oxime ether compound having a novel structure as shown in the general formula I. Respective substituents in the general formula I as defined in the specification. The compound of the general formula I exhibits an excellent microbicidal activity, and can effectively prevent and treat plant diseases caused by bacteria and fungi. Also provided is a use of the compound of the general formula I as a microbicide in the agricultural and other fields.

NOVEL CYCLIC COMPOUND HAVING QUINOLYLALKYLTHIO GROUP

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Page/Page column 16, (2010/11/28)

The present invention relates to a synthesis study of novel cyclic compounds having a quinolylalkylthio group represented by the formula (1), and pharmacological actions of the compounds. In the formula, the ring X represents: which may have halogen and/or alkyl; R1 and R2 independently represent hydrogen, alkyl, cycloalkyl, aryl or a (non) aromatic heterocycle; R3 represents qinolyl; A represents sulfur, sulfinyl or sulfonyl; and B represents alkylene.

Substituted alkylamine derivatives and methods of use

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Page 98, (2010/02/05)

Selected amines are effective for prophylaxis and treatment of diseases, such as angiogenesis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

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