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1H-Isoindol-1-one, 4-chloro-2-cyclooctyl-2,3-dihydro-5-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153144-47-9

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153144-47-9 Usage

Structure

Contains an isoindol-1-one ring, a chlorine atom, a cyclooctyl group, and a methoxy group.

Appearance

White to off-white crystalline solid.

Melting point

121-123°C.

Potential applications

Pharmaceutical research and development, particularly in the study of central nervous system disorders.

Note

Further research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 153144-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,4 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 153144-47:
(8*1)+(7*5)+(6*3)+(5*1)+(4*4)+(3*4)+(2*4)+(1*7)=109
109 % 10 = 9
So 153144-47-9 is a valid CAS Registry Number.

153144-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2-cyclooctyl-5-methoxy-2,3-dihydro-isoindol-1-one

1.2 Other means of identification

Product number -
Other names -

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:153144-47-9 SDS

153144-47-9Upstream product

153144-47-9Relevant academic research and scientific papers

Effects of [(N-alkyl-1,3-dihydro-1-oxoisoindolin-5-yl)oxy]alkanoic acids on chloride transport in primary astroglial cultures

Waller,Wyrick,Park,Kemp,Smith

, p. 571 - 576 (1994)

It has been demonstrated that agents which inhibit chloride influx and, therefore, lower intracellular chloride levels in the astrocyte, a major cell type in the cerebral gray matter, inhibit astrocytic swelling in vitro and in vivo. Herein, we report additional examples of a series of [(N-alkyl-1,3- dihydro-1-oxoisoindolin-5-yl)oxy]alkanoic acids and their effects upon ion transport in primary rat astrocyte cultures. The 4-chloro-substituted 1- oxoisoindolines demonstrated superior astrocytic chloride influx inhibitory activity as compared to the 6-chloro and non-chlorinated analogs. The four- carbon acid side chain derivatives were more active than the three- and two- carbon analogs. The pharmacological profile of these compounds was examined with respect to inhibition of the Cl--Cl-/Cl--HCO3- anion exchanger and Na+-K+-2Cl cotransport mechanisms in glia, and the compounds were found to exhibit a similar profile to that of furosemide by inhibiting both transporters.

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