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115104-40-0

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115104-40-0 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

Chloroquinolines are a class of chemical compounds that contain a quinoline ring with a chlorine atom attached.

Explanation

These compounds have been found to inhibit the growth of the malaria parasite in the blood, making them useful in treating malaria.

Explanation

Research is being conducted to explore the potential of chloroquinolines in treating other diseases, such as cancer and autoimmune disorders.

Explanation

The specific properties and applications of 1-(3-(7-Chloro-2-Quinolinyl) Ethyl) are still being studied to determine its potential as a therapeutic agent.

Explanation

The compound's structure is characterized by the presence of these functional groups, which contribute to its pharmacological properties.

Explanation

Due to its potential therapeutic applications, 1-(3-(7-Chloro-2-Quinolinyl) Ethyl) is considered a compound of interest for further research and development.

Chemical Class

Chloroquinoline derivative

Pharmacological Properties

Antimalarial agents

Potential Applications

Cancer and autoimmune disorders treatment

Therapeutic Applications

Under investigation

Structure

Contains a quinoline ring, an ethyl group, and a chlorine atom

Research Status

Compound of interest

Check Digit Verification of cas no

The CAS Registry Mumber 115104-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115104-40:
(8*1)+(7*1)+(6*5)+(5*1)+(4*0)+(3*4)+(2*4)+(1*0)=70
70 % 10 = 0
So 115104-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H12ClNO/c19-16-7-5-15-6-9-17(20-18(15)11-16)8-4-13-2-1-3-14(10-13)12-21/h1-12H

115104-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(7-Chloro-2-quinolinyl)vinyl]benzaldehyde

1.2 Other means of identification

Product number -
Other names 3-[2-(5-nitro-furan-2-yl)-vinyl]-[1,2,4]oxadiazol-5-ylamine

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:115104-40-0 SDS

115104-40-0Relevant articles and documents

Synthesis, biological evaluations and computational studies of N-(3-(-2-(7-Chloroquinolin-2-yl)vinyl) benzylidene)anilines as fungal biofilm inhibitors

Khan, Firoz A. Kalam,Kaduskar, Rashmi N.,Patil, Rajesh,Patil, Rajendra H.,Ansari, Siddique Akber,Alkahtani, Hamad M.,Almehizia, Abdulrahman A.,Shinde, Devanand B.,Sangshetti, Jaiprakash N.

, p. 623 - 630 (2019)

In the present investigation, new chloroquinoline derivatives bearing vinyl benzylidene aniline substituents at 2nd position were synthesized and screed for biofilm inhibitory, antifungal and antibacterial activity. The result of biofilm inhibition of C.

Process for unsymmetrical dithioacetals and dithioketals

-

, (2008/06/13)

This invention relates to a novel process for preparing unsymmetrical dithioacetals and dithioketals from aryl aldehydes and ketones.

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