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Oxazole-2-carboxylic acid is a heterocyclic chemical compound characterized by the molecular formula C5H3NO3. It features an oxazole ring fused with a carboxylic acid functional group, which endows it with unique chemical properties and reactivity. Oxazole-2-carboxylic acid is recognized for its role in the pharmaceutical industry, particularly as a key building block in the synthesis of a variety of drug molecules. Its structural attributes and versatility make it an essential component in drug discovery and development, as well as in research and chemical synthesis. Moreover, Oxazole-2-carboxylic acid holds promise for the creation of novel compounds with biological activities in the realm of organic chemistry.

33123-68-1

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33123-68-1 Usage

Uses

Used in Pharmaceutical Industry:
Oxazole-2-carboxylic acid is utilized as a crucial building block for the synthesis of various drug molecules, contributing to the development of new pharmaceuticals with potential therapeutic applications.
Used in Drug Discovery and Development:
It serves as a valuable component in the discovery and development of new drugs, owing to its unique structure and reactivity, which can be leveraged to create molecules with specific biological activities.
Used in Research and Chemical Synthesis:
Oxazole-2-carboxylic acid is employed in research settings and chemical synthesis processes, where its properties can be explored and harnessed to create new compounds with potential applications in various fields.
Used in Organic Chemistry for the Creation of New Compounds:
It has potential applications in the field of organic chemistry, where it can be used to synthesize new compounds with biological activities, expanding the scope of chemical and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 33123-68-1 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, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33123-68:
(7*3)+(6*3)+(5*1)+(4*2)+(3*3)+(2*6)+(1*8)=81
81 % 10 = 1
So 33123-68-1 is a valid CAS Registry Number.

33123-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-methyl-1,3-oxazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-methyl-oxazole-2-carboxylic 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:33123-68-1 SDS

33123-68-1Downstream Products

33123-68-1Relevant academic research and scientific papers

FUNCTIONALIZED AMINOTRIAZINES

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Page/Page column 61, (2020/06/10)

The present invention relates to novel antagonists of the A2B adenosine receptor and pharmaceutical compositions comprising said antagonists as well as their uses for the treatment and prevention of disorders known to be susceptible to improvement by anta

SUBSTITUTED XANTHINES AND METHODS OF USE THEREOF

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Page/Page column 399; 400, (2014/09/29)

Compounds, compositions and methods are described for inhibiting the TRPC5 ion channel and disorders related to TRPC5.

SPIROHYDANTOIN COMPOUNDS AND THEIR USE AS SELECTIVE ANDROGEN RECEPTOR MODULATORS

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Page/Page column 87, (2013/09/12)

The present invention relates to a compound of formula (1-1 ) in free form or in pharmaceutically acceptable salt form in which the substituents are as defined in the specification; to its preparation, to its use as a medicament and to medicaments comprising it. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

NOVEL SPIROPIPERIDINE COMPOUNDS

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Page/Page column 13, (2011/06/23)

A compound of the formula: or a pharmaceutically acceptable salt thereof as well as a pharmaceutical composition, and a method for treating diabetes.

Cyclization of propargylic amides: Mild access to oxazole derivatives

Weyrauch, Jan P.,Hashmi, A. Stephen K.,Schuster, Andreas,Hengst, Tobias,Schetter, Stefanie,Littmann, Anna,Rudolph, Matthias,Hamzic, Melissa,Visus, Jorge,Rominger, Frank,Frey, Wolfgang,Bats, Jan W.

supporting information; experimental part, p. 956 - 963 (2010/06/12)

The substrate scope, the mechanistic aspects of the gold-catalyzed oxazole synthesis, and substrates with different aliphatic, aromatic, and functional groups in the side chain were investigated. Even molecules with several propargyl amide groups could easily be converted, delivering di- and trioxazoles with interesting optical properties. Furthermore, the scope of the gold(I)-catalyzed alkylidene synthesis was investigated. Further functionalizations of these isolable intermediates of the oxazole synthesis were developed and chelate ligands can be obtained. The use of Barluenga's reagent offers a new and mild access to the synthetically valuable iodoalkylideneoxazoles from propargylic amides, this reagent being superior to other sources of halogens.

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