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1089660-72-9

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1089660-72-9 Usage

Description

(E)-3-(2-chloro-4-((3-(2,6-dichlorophenyl)-5-isopropylisoxazol-4-yl)methoxy)styryl)benzoic acid is a complex organic compound with a benzoic acid core, a styryl group, an isoxazole ring, and a chlorophenyl group. It also features chlorine and isopropyl functional groups, making it a member of the styrylbenzoic acid derivatives class. (E)-3-(2-chloro-4-((3-(2,6-dichlorophenyl)-5-isopropylisoxazol-4-yl)methoxy)styryl)benzoic acid is primarily utilized in scientific research for the development of pharmaceuticals and the exploration of its potential biological activities, such as anti-inflammatory, anti-cancer, or antimicrobial properties.

Uses

Used in Pharmaceutical Research:
(E)-3-(2-chloro-4-((3-(2,6-dichlorophenyl)-5-isopropylisoxazol-4-yl)methoxy)styryl)benzoic acid is used as a research compound for the development of pharmaceuticals, leveraging its potential biological activities to create new therapeutic agents.
Used in Scientific Research for Biological Activities:
In the field of scientific research, this compound is used as a tool to study its anti-inflammatory, anti-cancer, or antimicrobial properties, which could lead to the discovery of novel treatments for various diseases and conditions.
Used in Chemical Synthesis:
(E)-3-(2-chloro-4-((3-(2,6-dichlorophenyl)-5-isopropylisoxazol-4-yl)methoxy)styryl)benzoic acid is also used in chemical synthesis processes, where its unique structure and functional groups can be employed to create new compounds with specific applications in various industries.
Used in Drug Discovery:
In the pharmaceutical industry, this compound is used as a lead molecule in drug discovery, where its structure and properties are further optimized to develop effective drugs targeting specific biological pathways or receptors.
Used in Material Science:
The unique structure of (E)-3-(2-chloro-4-((3-(2,6-dichlorophenyl)-5-isopropylisoxazol-4-yl)methoxy)styryl)benzoic acid also makes it a candidate for material science applications, where it could be used to develop new materials with specific properties, such as optical, electronic, or mechanical characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 1089660-72-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,9,6,6 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1089660-72:
(9*1)+(8*0)+(7*8)+(6*9)+(5*6)+(4*6)+(3*0)+(2*7)+(1*2)=189
189 % 10 = 9
So 1089660-72-9 is a valid CAS Registry Number.

1089660-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(E)-2-(2-Chloro-4-{[3-(2,6-dichlorophenyl)-5-isopropyl-1,2-oxa zol-4-yl]methoxy}phenyl)vinyl]benzoic acid

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:1089660-72-9 SDS

1089660-72-9Relevant articles and documents

Identification of a chemical tool for the orphan nuclear receptor FXR

Maloney,Parks,Haffner,Fivush,Chandra,Plunket,Creech,Moore,Wilson,Lewis,Jones,Willson

, p. 2971 - 2974 (2000)

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Assays for ligands for nuclear receptors

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Page/Page column 16, (2010/11/30)

The present invention includes nuclear receptor heterodimer and nuclear receptor-coactivator pepetide assays for identifying ligands for nuclear receptors, utilizing scintillation proximity and fluorescence resonance energy transfer (FRET), and methods of using identified ligands.

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