76504-49-9 Usage
Uses
Used in Pharmaceutical Applications:
[2-(3,3-dimethyl-2-phenyloxiran-2-yl)-2-oxoethylidene]diazenium is used as a nitric oxide donor for its potential vasodilatory and anti-inflammatory effects. [2-(3,3-dimethyl-2-phenyloxiran-2-yl)-2-oxoethylidene]diazenium's ability to release nitric oxide can be beneficial in treating various medical conditions where these effects are desired.
Used in Research and Development:
In the field of pharmaceutical research and development, [2-(3,3-dimethyl-2-phenyloxiran-2-yl)-2-oxoethylidene]diazenium is used as a subject of study to explore its potential applications and understand its properties. Due to its complex structure and potentially reactive nature, careful handling and study are required to harness its potential in pharmaceutical settings.
Used in Drug Delivery Systems:
Similar to gallotannin, [2-(3,3-dimethyl-2-phenyloxiran-2-yl)-2-oxoethylidene]diazenium may also benefit from novel drug delivery systems to enhance its applications and efficacy. Researchers can explore the use of organic and metallic nanoparticles as carriers for [2-(3,3-dimethyl-2-phenyloxiran-2-yl)-2-oxoethylidene]diazenium, aiming to improve its delivery, bioavailability, and therapeutic outcomes in various medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 76504-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,0 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76504-49:
(7*7)+(6*6)+(5*5)+(4*0)+(3*4)+(2*4)+(1*9)=139
139 % 10 = 9
So 76504-49-9 is a valid CAS Registry Number.
76504-49-9Relevant 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.
