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23244-34-0

5-Ethoxy-3-phenylisoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 23244-34-0 Structure

  • Basic information

    1. Product Name: 5-Ethoxy-3-phenylisoxazole
    2. Synonyms: 5-Ethoxy-3-phenylisoxazole
    3. CAS NO:23244-34-0
    4. Molecular Formula: C11H11NO2
    5. Molecular Weight: 189.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23244-34-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Ethoxy-3-phenylisoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Ethoxy-3-phenylisoxazole(23244-34-0)
    11. EPA Substance Registry System: 5-Ethoxy-3-phenylisoxazole(23244-34-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 23244-34-0(Hazardous Substances Data)

23244-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23244-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,4 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23244-34:
(7*2)+(6*3)+(5*2)+(4*4)+(3*4)+(2*3)+(1*4)=80
80 % 10 = 0
So 23244-34-0 is a valid CAS Registry Number.

23244-34-0SDS

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 5-ethoxy-3-phenyl-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 3-Phenyl-5-ethyoxyisoxazol

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:23244-34-0 SDS

23244-34-0Relevant articles and documents

General Platform for the Conversion of Isoxazol-5-ones to 3,5-Disubstituted Isoxazoles via Nucleophilic Substitutions and Palladium Catalyzed Cross-Coupling Strategies

Fernandes, Alessandra A. G.,da Silva, Amanda F.,Okada, Celso Y.,Suzukawa, Vitor,Cormanich, Rodrigo A.,Jurberg, Igor D.

, p. 3022 - 3034 (2019/05/17)

A general platform for the conversion of isoxazol-5-ones to 3,5-disubstituted isoxazoles has been developed via a two-step strategy. The first step leads to the formation of 5-(pseudo)halogenated isoxazoles, while in the second, a variety of heteroalkyl-, heteroaryl-, alkyl-, alkenyl-, alkynyl- and aryl-chains can be installed via nucleophilic substitutions or palladium catalyzed cross-coupling reactions.

4-Alkoxy-3-cyano-2(1H)-pyridones and 5-alkoxyisoxazoles and their aryl substituted and annulated derivatives from acylketene O,S-acetals

Purkayastha,Bhat,Ila,Junjappa

, p. 641 - 643 (2007/10/02)

The title pyridones 2 and 5 and the isoxazoles 3 and 6 are obtained in moderate to good yields by cyclocondensation of the appropriate acylketene O,S-acetals 1 or 4 with cyanoacetamide and hydroxylamine hydrochloride, respectively, in the presence of sodi

NUCLEOPHILIC DISPLACEMENT OF THE METHOXY GROUP IN 5-METHOXYISOXAZOLE

Auricchio, Sergio,Ricca, Aldo,Truscello, Ada M.

, p. 297 - 298 (2007/10/02)

The reaction of 5-methoxy-3-phenylisoxazole, 1a, with primary and secondary alcohols in the presence of acids gives 5-alkoxy derivatives 1b-d in almost quantitative yields.

SYNTHESIS OF ISOXAZOLINES AND ISOXAZOLES FROM ALDOXIMES BY THE USE OF SODIUM BROMITE WITH ORGANOTIN HALIDE

Moriya, Osamu,Nakamura, Hideki,Kageyama, Toshifumi,Urata, Yoshikiya

, p. 3987 - 3990 (2007/10/02)

The oxidizing system using sodium bromite with a catalytic amount of tri-n-butyltin chloride is applied for the preparations of isoxazolines and isoxazoles from aldoximes via dipolar cycloaddition.

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