14650-51-2 Usage
Uses
Used in Pharmaceutical Applications:
[1-(ethoxycarbonyl)-2-oxo-3-phenoxypropylidene]diazenium is used as a pharmaceutical agent for its controlled and sustained release of nitric oxide (NO). [1-(ethoxycarbonyl)-2-oxo-3-phenoxypropylidene]diazenium's ability to deliver NO in a targeted manner can be beneficial for various therapeutic applications, such as vasodilation and other NO-related treatments.
Used in Drug Delivery Systems:
In the field of drug delivery, [1-(ethoxycarbonyl)-2-oxo-3-phenoxypropylidene]diazenium is used as a carrier for targeted NO delivery. The presence of the ethoxycarbonyl and phenoxypropylidene groups may enhance the compound's chemical reactivity and specificity, making it a promising candidate for improving drug delivery efficiency and therapeutic outcomes.
Used in Research and Development:
[1-(ethoxycarbonyl)-2-oxo-3-phenoxypropylidene]diazenium is used as a research tool for studying the role of nitric oxide in various biological processes and its potential applications in medicine. [1-(ethoxycarbonyl)-2-oxo-3-phenoxypropylidene]diazenium's controlled NO release and unique structural features make it a valuable asset for exploring new therapeutic strategies and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 14650-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,5 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14650-51:
(7*1)+(6*4)+(5*6)+(4*5)+(3*0)+(2*5)+(1*1)=92
92 % 10 = 2
So 14650-51-2 is a valid CAS Registry Number.
14650-51-2Relevant academic research and scientific papers
Rh-catalyzed intramolecular aromatic C-H insertion of α-diazo β-ketoesters: Synthesis of 4-carbonyl chroman derivatives
Zhang, Xiaolin,Lei, Mei,Zhang, Yi-Nan,Hu, Li-Hong
, p. 3400 - 3406 (2014/05/06)
A Rh-catalyzed intramolecular aromatic C-H insertion of α-diazo β-ketoesters was developed. This protocol offers a practical strategy for the synthesis of 4-carbonyl chroman derivatives with high yield and is compatible with a wide variety of substituents
Metal substituted diazo esters as substrates for cross coupling reactions
Padwa, Albert,Sa, Marcus M.,Weingarten, M. David
, p. 2371 - 2386 (2007/10/03)
Ethyl (trialkylstannyl)diazoacetates have been employed as substrates in the Stille reaction, The palladium(O)-catalyzed cross coupling works well with aryl iodides but not with acyl or aryl chlorides. Bis-[ethoxycarbonyl-diazomethyl]-mercury showed high
