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5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is a chemical compound characterized by the molecular formula C13H10N2O5. It is an ethyl ester derivative of oxazole-4-carboxylic acid, featuring a nitrophenyl group attached to the 5th position of the oxazole ring. 5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER holds potential in the realm of medicinal chemistry and drug development due to its distinctive structural and chemical properties, making it a promising candidate for the exploration of novel pharmaceuticals and biologically active substances.

72030-87-6

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72030-87-6 Usage

Uses

Used in Medicinal Chemistry Research:
5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is utilized as a research compound for the development of new pharmaceuticals. Its unique structure and properties contribute to its potential as a precursor or intermediate in the synthesis of biologically active molecules.
Used in Drug Development:
In the pharmaceutical industry, 5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is employed as a key component in the design and synthesis of innovative drugs. Its chemical versatility allows for the creation of diverse drug candidates that could address various medical conditions.
Further studies and investigations are essential to fully comprehend the potential applications and effects of 5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER, ensuring its safe and effective use in future therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 72030-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,3 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72030-87:
(7*7)+(6*2)+(5*0)+(4*3)+(3*0)+(2*8)+(1*7)=96
96 % 10 = 6
So 72030-87-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2O5/c1-2-18-12(15)10-11(19-7-13-10)8-3-5-9(6-4-8)14(16)17/h3-7H,2H2,1H3

72030-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-(4-nitrophenyl)oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-(4-nitrophenyl)-1,3-oxazole-4-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72030-87-6 SDS

72030-87-6Relevant academic research and scientific papers

Synthesis and evaluation of potent and selective β3 adrenergic receptor agonists containing heterobiaryl carboxylic acids

Shearer, Barry G.,Chao, Esther Y.,Uehling, David E.,Deaton, David N.,Cowan, Conrad,Sherman, Bryan W.,Milliken, Tula,Faison, Walter,Brown, Kathleen,Adkison, Kimberly K.,Lee, Frank

, p. 4670 - 4677 (2008/02/12)

The design, synthesis, and SAR of a novel series of heterobiaryl phenethanolamine β3 adrenergic receptor agonists are described. The furan analogue 49 was shown to elicit a significant dose-dependent lowering of plasma glucose in a rodent model

Fully automated continuous flow synthesis of 4,5-disubstituted oxazoles

Baumann, Marcus,Baxendale, Ian R.,Ley, Steven V.,Smith, Christoper D.,Tranmer, Geoffrey K.

, p. 5231 - 5234 (2007/10/03)

A multipurpose mesofluidic flow reactor capable of producing gram quantities of material has been developed as an automated synthesis platform for the rapid on-demand synthesis of key building blocks and small exploratory libraries. The reactor is configu

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