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[2-(4-nitrophenoxy)-2-oxoethylidene]diazenium is a chemical compound with the formula C8H5N4O3, belonging to the class of diazeniumdiolates. It is derived from the reaction of a diazeniumdiolate moiety with a 4-nitrophenoxy group, and is known for its potential use as a nitric oxide (NO) donor. Nitric oxide is a crucial signaling molecule in the body, playing a significant role in various physiological processes, which makes [2-(4-nitrophenoxy)-2-oxoethylidene]diazenium and related compounds promising candidates for pharmaceutical applications.

28293-55-2

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28293-55-2 Usage

Uses

Used in Pharmaceutical Applications:
[2-(4-nitrophenoxy)-2-oxoethylidene]diazenium is used as a nitric oxide (NO) donor for its potential pharmaceutical applications. [2-(4-nitrophenoxy)-2-oxoethylidene]diazenium can release NO in physiological conditions, which is an essential signaling molecule involved in multiple physiological processes. This property makes it a promising candidate for the development of drugs targeting various health conditions.
Used in Research and Development:
In the field of scientific research, [2-(4-nitrophenoxy)-2-oxoethylidene]diazenium is used as a research compound to study the effects of nitric oxide in biological systems. Its ability to release NO under physiological conditions allows researchers to investigate the role of NO in cellular processes and develop a better understanding of its implications in health and disease.
Used in Drug Delivery Systems:
Similar to gallotannin, [2-(4-nitrophenoxy)-2-oxoethylidene]diazenium can be employed in the development of novel drug delivery systems to enhance its applications and efficacy. By incorporating [2-(4-nitrophenoxy)-2-oxoethylidene]diazenium into various organic and metallic nanoparticles, researchers aim to improve its delivery, bioavailability, and therapeutic outcomes in targeted applications.
Used in Application Industry:
[2-(4-nitrophenoxy)-2-oxoethylidene]diazenium is used as a nitric oxide donor in the pharmaceutical industry for the development of drugs targeting various health conditions. Its ability to release NO in physiological conditions makes it a valuable compound for creating innovative therapeutic solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 28293-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,9 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28293-55:
(7*2)+(6*8)+(5*2)+(4*9)+(3*3)+(2*5)+(1*5)=132
132 % 10 = 2
So 28293-55-2 is a valid CAS Registry Number.

28293-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-diazonio-1-(4-nitrophenoxy)ethenolate

1.2 Other means of identification

Product number -
Other names p-nitrophenyl diazoacetate

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:28293-55-2 SDS

28293-55-2Relevant academic research and scientific papers

Design and synthesis of active heparan sulfate-based probes

Zhou, Wen,Hsieh, Po-Hung,Xu, Yongmei,O'Leary, Timothy R.,Huang, Xuefei,Liu, Jian

supporting information, p. 11019 - 11021 (2015/07/02)

A chemoenzymatic approach for synthesizing heparan sulfate oligosaccharides with a reactive diazoacetyl saccharide residue is reported. The resultant oligosaccharides were demonstrated to serve as specific inhibitors for heparan sulfate sulfotransferases,

Chemistry of diazopolycarbonyl compounds: V. Synthesis, structure, and chemical characteristics of aryl diazoacetates

Zalesov,Kataev

, p. 1666 - 1672 (2007/10/03)

Aryl diazoacetates were prepared, and basing on spectral data and quantum-chemical calculations cis-trans isomerism thereof was proved. The reactions of diazoesters with hydrochloric and sulfuric acids, triphenylphosphine, and dinitrogen tetroxide resulted respectively in aryl chloroacetates, bis(aryloxy-carbonylmethyl) sulfates, triphenylphosphoranylidenehydrazones of aryl 2-oxoethanoates, and N-oxides of diaryl 1,2,5-oxadiazole-3,4-dicarboxylates.

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