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[2-(2,3-diphenyloxiran-2-yl)-2-oxoethylidene]diazenium is a complex chemical compound that belongs to the class of diazo derivatives. It features a diazenium group, an oxiran ring, and a ketone group in its structure. This reactive compound has the potential to participate in various chemical reactions, suggesting its utility in organic synthesis, pharmaceuticals, and material science. The presence of a diazenium group also hints at possible applications as a nitric oxide donor or a nitric oxide-releasing compound with potential pharmacological activity.

53884-91-6

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53884-91-6 Usage

Uses

Used in Organic Synthesis:
[2-(2,3-diphenyloxiran-2-yl)-2-oxoethylidene]diazenium is used as a reactive intermediate for the synthesis of various complex organic molecules. Its unique structure allows for the formation of new chemical bonds and the creation of diverse molecular architectures.
Used in Pharmaceutical Applications:
[2-(2,3-diphenyloxiran-2-yl)-2-oxoethylidene]diazenium is used as a potential nitric oxide-releasing compound in the pharmaceutical industry. Nitric oxide is a signaling molecule that plays a crucial role in various physiological processes. [2-(2,3-diphenyloxiran-2-yl)-2-oxoethylidene]diazenium's ability to release nitric oxide may lead to the development of new drugs targeting conditions related to nitric oxide dysregulation.
Used in Material Science:
[2-(2,3-diphenyloxiran-2-yl)-2-oxoethylidene]diazenium is used as a building block for the development of novel materials with specific properties. Its unique structure and reactivity can contribute to the creation of materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials for energy storage and conversion.
Ongoing Research:
Studies on the properties and potential uses of [2-(2,3-diphenyloxiran-2-yl)-2-oxoethylidene]diazenium are ongoing. Further research is necessary to fully understand its characteristics, optimize its synthesis, and explore its applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 53884-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,8 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53884-91:
(7*5)+(6*3)+(5*8)+(4*8)+(3*4)+(2*9)+(1*1)=156
156 % 10 = 6
So 53884-91-6 is a valid CAS Registry Number.

53884-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-2-diazonio-1-(2,3-diphenyloxiran-2-yl)ethenolate

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 -
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More Details:53884-91-6 SDS

53884-91-6Relevant academic research and scientific papers

SYNTHESIS OF α,β-EPOXY DIAZOMETHYL KETONES

Thijs, L.,Smeets, F. L. M.,Cillissen, P. J. M.,Harmsen, J.,Zwanenburg, B.

, p. 2141 - 2144 (2007/10/02)

The preparation of eighteen epoxy diazomethyl ketones 1 is described.Two general methods were developed.Firstly, treatment of the mixed anhydrides of glycidic acids and carbonic acid ester with diazomethane led to the title compounds in yields ranging from 17-74 percent.Secondly, glycidyl chlorides which were obtained from sodium glycidates and oxalyl chloride, gave the desired products upon treatment with diazomethane ( yields 60-74 percent).The required α,β-epoxy carboxylic esters were prepared by Darzens condensation and epoxidation of α,β-unsaturated esters, but in some cases also by reaction of α-oxo carboxylic esters with diazomethane.

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