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

66692-93-1

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66692-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66692-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,9 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66692-93:
(7*6)+(6*6)+(5*6)+(4*9)+(3*2)+(2*9)+(1*3)=171
171 % 10 = 1
So 66692-93-1 is a valid CAS Registry Number.

66692-93-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(p-methoxyphenyl)-4-nitro-5-phenylisoxazole

1.2 Other means of identification

Product number -
Other names 3-(4-Methoxy-phenyl)-4-nitro-5-phenyl-isoxazol

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:66692-93-1 SDS

66692-93-1Downstream Products

66692-93-1Relevant academic research and scientific papers

Synthesis of 4-Nitroisoxazoles via NO/NO2 -Mediated Heterocyclization of Aryl-Substituted α,β-Unsaturated Ketones

Averina, Elena B.,Grishin, Yuri K.,Kurova, Anastasiya V.,Kuznetsova, Tamara S.,Rybakov, Victor B.,Sadovnikov, Kirill S.,Sedenkova, Kseniya N.,Vasilenko, Dmitry A.,Volkova, Yulia A.

, p. 1398 - 1406 (2020)

A straightforward approach for the synthesis of 4-nitroisoxazoles has been developed via heterocyclization of aryl/hetaryl-substituted α,β-unsaturated ketones upon treatment with tetranitromethane-triethylamine (TNM-TEA) complex or t -BuONO. This strategy features high efficiency and wide substrate tolerance under simple reaction conditions.

SYNTHESIS AND PROPERTIES OF AZOLES AND THEIR DERIVATIVES. PART XX. STUDIES ON THE THERMOLYSIS OF REGIO AND STEREOISOMERIC DIARYLNITRO-Δ2-ISOXAZOLINES

Baranski, Andrzej,Cholewka, Elzbieta

, p. 483 - 494 (2007/10/02)

Thermolysis of stereoisomeric 3,5-diaryl-4-nitro-Δ2-isoxazolines 1, 3, depending on the applied solvent, leads to 3,5-diarylisoxazoles 4 or mixtures of 3,5-diarylisoxazoles 4 and 3,5-diaryl-4-nitroisoxazoles 6.Under similar conditions, 3,4-diar

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