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3-(2-BROMO-PHENYL)-ISOXAZOLE-5-CARBOXYLIC ACID ETHYL ESTER is a chemical compound with the molecular formula C12H9BrN2O3. It is an organic compound that belongs to the class of isoxazole derivatives, which are known for their diverse biological activities. This specific compound is an ethyl ester, indicating that it contains an ethyl group attached to the carboxylic acid functional group. The presence of the 2-bromo-phenyl group suggests potential reactivity and possible use in pharmaceutical or agrochemical applications. 3-(2-BROMO-PHENYL)-ISOXAZOLE-5-CARBOXYLIC ACID ETHYL ESTER's structural features also indicate the potential for use as a building block in organic synthesis or as a precursor in the development of new pharmaceutical compounds.

885273-64-3

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885273-64-3 Usage

Uses

Used in Pharmaceutical Industry:
3-(2-BROMO-PHENYL)-ISOXAZOLE-5-CARBOXYLIC ACID ETHYL ESTER is used as a building block for the synthesis of pharmaceutical compounds due to its diverse biological activities and potential reactivity.
Used in Agrochemical Industry:
3-(2-BROMO-PHENYL)-ISOXAZOLE-5-CARBOXYLIC ACID ETHYL ESTER is used as a precursor in the development of new agrochemical compounds, leveraging its potential reactivity and structural features.
Used in Organic Synthesis:
3-(2-BROMO-PHENYL)-ISOXAZOLE-5-CARBOXYLIC ACID ETHYL ESTER is used as a starting material in organic synthesis, enabling the creation of various complex organic molecules for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 885273-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 885273-64:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*3)+(2*6)+(1*4)=213
213 % 10 = 3
So 885273-64-3 is a valid CAS Registry Number.

885273-64-3SDS

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 ethyl 3-(2-bromophenyl)-1,2-oxazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names ETHYL 3-(2-BROMOPHENYL)ISOXAZOLE-5-CARBOXYLATE

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

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More Details:885273-64-3 SDS

885273-64-3Downstream Products

885273-64-3Relevant academic research and scientific papers

Alkyl Nitrites: Novel Reagents for One-Pot Synthesis of 3,5-Disubstituted Isoxazoles from Aldoximes and Alkynes

Kadam, Kishorkumar S.,Gandhi, Thirumanavelan,Gupte, Amol,Gangopadhyay,Sharma, Rajiv

, p. 3996 - 4008 (2016)

An efficient, one-pot approach has been described for the synthesis of 3,5-disubstituted isoxazoles from substituted aldoximes (mixture of E and Z) and alkynes, using alkyl nitrites under conventional heating conditions. The key nitrile oxide intermediates that are required for the synthesis of isoxazoles are formed by treatment of substituted aldoxime with either tert-butyl nitrite or isoamyl nitrite. The generated nitrile oxides underwent in situ [3+2] dipolar cycloaddition to the substituted alkynes to give 3,5-disubstituted isoxazoles regioselectively in high to excellent yields. The developed synthetic methodology was applied for the synthesis of a previously reported potent hDGAT1 inhibitor.

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