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2-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is a nitrophenyl-substituted oxazole compound that plays a significant role in organic synthesis and chemical research. Its unique structure and reactivity contribute to its value in creating a variety of functionalized molecules and complex organic compounds. It is commonly used as an intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential hazards, it is crucial to handle this chemical with care, adhering to proper safety protocols and regulations.

78979-63-2

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78979-63-2 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as an intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is utilized as an intermediate in the production of agrochemicals. Its reactivity and functional groups enable the creation of compounds with targeted effects on pests and diseases, enhancing crop protection and yield.
Used in Specialty Chemicals Production:
2-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as an intermediate in the synthesis of specialty chemicals. Its versatility in forming diverse functionalized molecules makes it valuable for creating compounds with specific applications in various industries, such as materials science, coatings, and dyes.
Used in Organic Synthesis Research:
As a key component in organic synthesis research, 2-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is employed to explore new reaction pathways and develop innovative synthetic methods. Its unique properties provide opportunities for researchers to investigate novel chemical transformations and expand the scope of organic chemistry.
Used in Chemical Education:
2-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER can be utilized as a teaching aid in chemical education. Its reactivity and structural features offer a platform for students to understand the principles of organic synthesis and the importance of intermediates in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 78979-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,7 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78979-63:
(7*7)+(6*8)+(5*9)+(4*7)+(3*9)+(2*6)+(1*3)=212
212 % 10 = 2
So 78979-63-2 is a valid CAS Registry Number.

78979-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(4-nitrophenyl)-1,3-oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:78979-63-2 SDS

78979-63-2Downstream Products

78979-63-2Relevant academic research and scientific papers

A silver-mediated one-step synthesis of oxazoles

Ritson, Dougal J.,Spiteri, Christian,Moses, John E.

supporting information; experimental part, p. 3519 - 3522 (2011/06/24)

A silver-mediated one-step procedure to 2,4-disubstituted and 2,4,5-trisubstituted oxazoles has been developed. The method is complementary to existing technologies, yet provides advantages with regard to simplicity, efficiency, and performance. The silver product can be readily recycled, thus minimizing waste.

Synthesis of Oxazolidines, Thiazolidines, and 5,6,7,8-Tetrahydro-1H,3H-pyrrolooxazole (or thiazole)-1,3-diones from β-Hydroxy- or β-Mercapto-α-amino Acid Esters

Badr, Mahmoud Zarif Amin,Aly, Morsy Mohamed,Fahmy, Atiat Mohamed,Mansour, Mansour Esmael Younis

, p. 1844 - 1847 (2007/10/02)

2-Aryl-4-(ethoxycarbonyl)oxazolidines and thiazolidines (1) were prepared from the corresponding α-amino acid ethyl esters containing either hydroxyl or mercapto groups in the β position by fusion with some aromatic aldehydes.Dehydrogenation of 1 with N-b

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