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Isoxazole, 5-(4-chlorophenyl)-3-(4-Methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24097-20-9

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24097-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24097-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24097-20:
(7*2)+(6*4)+(5*0)+(4*9)+(3*7)+(2*2)+(1*0)=99
99 % 10 = 9
So 24097-20-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H12ClNO2/c1-19-14-8-4-11(5-9-14)15-10-16(20-18-15)12-2-6-13(17)7-3-12/h2-10H,1H3

24097-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-chlorophenyl)-3-(4-methoxyphenyl)-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 5-(4-chloro-phenyl)-3-(4-methoxy-phenyl)-isoxazole

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:24097-20-9 SDS

24097-20-9Relevant academic research and scientific papers

O-iodoxy benzoic acid–mediated synthesis of 3,5-diarylisoxazoles and isoxazole-3-carboxylic acids

Desai, Vidya G.,Naik, Sneha R.,Dhumaskar, Kashinath L.

, p. 1453 - 1460 (2016/09/23)

A new, convenient, ecofriendly synthesis of 3,5-diarylisoxazoles is reported from a,b-unsaturated ketoximes. Similarly, a novel synthesis of isoxazole carboxylic acids is also reported. Both the methods use efficient, environmentally friendly, and nontoxic iodoxybenzoic acid (IBX) as an oxidative cyclizing reagent. Easy procedure, environmentally benign reaction conditions, and nontoxicity are advantages to the methodology.

Synthesis of 3,5-diarylisoxazoles under solvent-free conditions using iodobenzene diacetate

Chandra Sekhar, Kondapalli Venkata Gowri,Sasank, Thripuraribhatla Venkata Naga Varuna Tara,Nagesh, Hunsur Nagendra,Suresh, Narva,Naidu, Kalaga Mahalakshmi,Suresh, Amaroju

, p. 1045 - 1048 (2014/01/06)

A simple and efficient method has been developed for conversion of chalcone oximes to 3,5-diaryl isoxazoles in excellent yields under solvent-free conditions. The synthesized compounds were characterized by infrared spectroscopy, 1H NMR, 13C NMR and HRMS.

Exploration of the SAR of anti-invasive chalcones: Synthesis and biological evaluation of conformationally restricted analogues

Roman, Bart I.,Ryck, Tine De,Dierickx, Laura,Vanhoecke, Barbara W.A.,Katritzky, Alan R.,Bracke, Marc,Stevens, Christian V.

, p. 4812 - 4819 (2012/09/08)

In order to get a clearer view on the active geometry of anti-invasive chalcones, we have prepared a number of isoxazoles and related substances as conformationally restrained mimics of 1,3-diarylpropenones, and also of (Z)-stilbenes. In vitro anti-invasi

Synthesis and structure-activity relationships of 3,5-diarylisoxazoles and 3,5-diaryl-1,2,4-oxadiazoles, novel classes of small molecule interleukin-8 (IL-8) receptor antagonists

Weidner-Wells, Michele A.,Henninger, Todd C.,Fraga-Spano, Stephanie A.,Boggs, Christine M.,Matheis, Michele,Ritchie, David M.,Argentieri, Dennis C.,Wachter, Michael P.,Hlasta, Dennis J.

, p. 4307 - 4311 (2007/10/03)

A novel series of 3,5-diarylisoxazole and 3,5-diaryl-1,2,4-oxadiazole IL-8 inhibitors has been identified. These compounds exhibit activity in an IL-8 binding assay as well as in a functional assay of IL-8 induced elastase release from neutrophils. In add

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