3490-50-4 Usage
Description
[2-(4-cyanophenyl)-2-oxoethylidene]diazenium is a chemical compound that contains a diazenium structure and a cyanophenyl group. It is a diazeniumdiolate, which means it contains a nitric oxide donor group. Diazeniumdiolates are known for their ability to release nitric oxide, a signaling molecule with a wide range of physiological and pharmacological effects. The cyanophenyl group is a common functional group in organic chemistry, and its presence in this compound indicates potential applications in medicinal chemistry and drug development. Overall, [2-(4-cyanophenyl)-2-oxoethylidene]diazenium is a compound with potential biological activity due to its nitric oxide-releasing properties and its cyanophenyl group, making it of interest for further study in the fields of pharmacology and medicinal chemistry.
Uses
Used in Pharmaceutical Applications:
[2-(4-cyanophenyl)-2-oxoethylidene]diazenium is used as a pharmaceutical agent for its nitric oxide-releasing properties. Nitric oxide is a signaling molecule that plays a crucial role in various physiological processes, including vasodilation, neurotransmission, and immune response regulation. [2-(4-cyanophenyl)-2-oxoethylidene]diazenium's ability to release nitric oxide may provide therapeutic benefits in treating conditions related to nitric oxide dysregulation.
Used in Medicinal Chemistry Research:
[2-(4-cyanophenyl)-2-oxoethylidene]diazenium is used as a research tool in medicinal chemistry for its potential to develop new drugs targeting nitric oxide pathways. The cyanophenyl group in the compound may offer opportunities for structural modifications and optimization to enhance its biological activity and pharmacological properties.
Used in Drug Delivery Systems:
In the field of drug delivery, [2-(4-cyanophenyl)-2-oxoethylidene]diazenium can be used as a component in the development of novel drug delivery systems. Its nitric oxide-releasing properties and cyanophenyl group may enable the design of targeted drug delivery systems that can improve the bioavailability and therapeutic efficacy of the compound.
Used in Chemical Synthesis:
[2-(4-cyanophenyl)-2-oxoethylidene]diazenium can be used as a synthetic building block in the development of new chemical compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals. The cyanophenyl group and diazenium structure provide opportunities for further chemical modifications and the creation of new molecules with desired properties.
Check Digit Verification of cas no
The CAS Registry Mumber 3490-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3490-50:
(6*3)+(5*4)+(4*9)+(3*0)+(2*5)+(1*0)=84
84 % 10 = 4
So 3490-50-4 is a valid CAS Registry Number.
3490-50-4Relevant articles and documents
Phosphoric Acid Catalyzed [4 + 1]-Cycloannulation Reaction of ortho-Quinone Methides and Diazoketones: Catalytic, Enantioselective Access toward cis-2,3-Dihydrobenzofurans
Suneja, Arun,Schneider, Christoph
supporting information, p. 7576 - 7580 (2019/01/03)
A highly straightforward route to enantiomerically highly enriched cis-2,3-dihydrobenzofurans has been achieved via addition of α-diazocarbonyl compounds to in situ generated o-QMs catalyzed by a chiral Br?nsted acid. This catalytic strategy provides a direct access to 2,3-dihydrobenzofurans in high yields and with up to 91:9 dr and 99:1 er at ambient temperature. Moreover, a unique phenonium-type rearrangement accounts for product formation with an inverted 2,3-substitution pattern.
Amination of phenylketene revisit. Substituent effect on reactivity
Badal, Md. Mizanur Rahman,Zhang, Min,Kobayashi, Shinjiro,Mishima, Masaaki
, p. 856 - 863 (2013/08/15)
The asymmetric stretching frequencies of the ketene group of the m,p-substituted phenylketenes were found to be correlated with σ The substituent effects for the second-order rate constants of phenylketenes with various amines were not correlated linearly
Synthesis of amidinophenylacetic acids and amidinophenyl-alpha-amino-acetic acids
Richter,Garbe,Wagner
, p. 256 - 262 (2007/10/06)
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