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5-tert-Butyl-2-oxazolecarboxylic Acid Ethyl Ester is an organic compound that belongs to the class of oxazole carboxylic acid esters. It is characterized by the presence of a tert-butyl group and an ethyl ester functional group, which contribute to its chemical properties and potential applications in various industries.

33123-71-6

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33123-71-6 Usage

Uses

Used in Pharmaceutical Industry:
5-tert-Butyl-2-oxazolecarboxylic Acid Ethyl Ester is used as a synthetic intermediate for the development of more complex pharmaceutical and biologically active compounds. Its unique structural features make it a valuable building block in the synthesis of novel drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 5-tert-Butyl-2-oxazolecarboxylic Acid Ethyl Ester serves as a versatile compound for exploring new reaction pathways and understanding the reactivity of oxazole carboxylic acid esters. This knowledge can be applied to design and synthesize new molecules with specific properties and functions.
Used in Material Science:
5-tert-Butyl-2-oxazolecarboxylic Acid Ethyl Ester can be utilized in the development of novel materials with tailored properties. Its incorporation into polymers or other materials can lead to improved performance characteristics, such as enhanced stability, reactivity, or selectivity in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 33123-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,2 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33123-71:
(7*3)+(6*3)+(5*1)+(4*2)+(3*3)+(2*7)+(1*1)=76
76 % 10 = 6
So 33123-71-6 is a valid CAS Registry Number.

33123-71-6SDS

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-tert-butyl-oxazole-2-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 5-tert-Butyl-2-oxazolecarboxylic Acid Ethyl Ester

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:33123-71-6 SDS

33123-71-6Relevant academic research and scientific papers

Development of a continuous flow photoisomerization reaction converting isoxazoles into diverse oxazole products

Bracken, Cormac,Baumann, Marcus

, p. 2607 - 2617 (2020/03/11)

A continuous flow process is presented, which directly converts isoxazoles into their oxazole counterparts via a photochemical transposition reaction. This results in the first reported exploitation of this transformation to establish its scope and synthe

Silver-Induced [3+2] Cycloaddition of Isocyanides with Acyl Chlorides: Regioselective Synthesis of 2,5-Disubstituted Oxazoles

Liu, Jian-Quan,Shen, Xuanyu,Shatskiy, Andrey,Zhou, Enlong,K?rk?s, Markus D.,Wang, Xiang-Shan

, p. 4272 - 4275 (2019/07/19)

A silver-induced cycloaddition of isocyanides with acyl chlorides has been developed. This transition metal-catalyzed strategy provides an effective and scalable approach for the formation of 2,5-disubstituted oxazoles in good to high yields. The employed silver-based MOF catalyst can be efficiently recycled without compromising the yield.

Oxazole carboxamide herbicides

-

, (2008/06/13)

The novel compounds of formula I: wherein R1, R2, R3, R4 and Ar have the meaning given in claim 1, and herbicidal compositions containing such compounds as active ingredients.

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