1807-69-8 Usage
Description
[2-methoxy-2-oxo-1-(phenylcarbonyl)ethylidene]diazenium, a diazeniumdiolate derivative with the chemical formula C10H10N2O3, is a chemical compound that has garnered attention for its potential applications in the medical and scientific fields. [2-methoxy-2-oxo-1-(phenylcarbonyl)ethylidene]diazenium is recognized for its anti-inflammatory, anti-cancer, and antibacterial properties, making it a promising candidate for therapeutic interventions.
Uses
Used in Pharmaceutical Applications:
[2-methoxy-2-oxo-1-(phenylcarbonyl)ethylidene]diazenium is used as a therapeutic agent for its anti-inflammatory, anti-cancer, and antibacterial properties. Its ability to inhibit the growth of various cancer cells and exhibit potential in the treatment of inflammatory diseases and bacterial infections makes it a valuable compound in the field of medicine and biochemistry.
Used in Cancer Treatment:
In the field of oncology, [2-methoxy-2-oxo-1-(phenylcarbonyl)ethylidene]diazenium is used as an anti-cancer agent. It has shown potential in targeting and inhibiting the growth of cancer cells, making it a promising candidate for further research and development in cancer treatment strategies.
Used in Inflammatory Disease Treatment:
The anti-inflammatory properties of [2-methoxy-2-oxo-1-(phenylcarbonyl)ethylidene]diazenium make it a candidate for use in the treatment of various inflammatory diseases. Its potential to alleviate inflammation and reduce associated symptoms could contribute to improved patient outcomes in this area.
Used in Antibacterial Applications:
Given its demonstrated antibacterial properties, [2-methoxy-2-oxo-1-(phenylcarbonyl)ethylidene]diazenium can be used as an agent in the fight against bacterial infections. Its potential to inhibit bacterial growth and reduce the spread of infections could be particularly useful in the development of new antibiotics and treatment strategies for drug-resistant bacteria.
Further research is necessary to fully understand the potential uses and effects of [2-methoxy-2-oxo-1-(phenylcarbonyl)ethylidene]diazenium, but its multifaceted properties suggest that it could become a versatile and valuable chemical in the field of medicine and biochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1807-69-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,0 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1807-69:
(6*1)+(5*8)+(4*0)+(3*7)+(2*6)+(1*9)=88
88 % 10 = 8
So 1807-69-8 is a valid CAS Registry Number.
1807-69-8Relevant articles and documents
Iridium(III)-Catalyzed C(3)-H Alkylation of Isoquinolines via Metal Carbene Migratory Insertion
Jha, Neha,Singh, Roushan Prakash,Saxena, Paridhi,Kapur, Manmohan
supporting information, p. 8694 - 8698 (2021/11/24)
An Ir(III)-catalyzed C(3)-H alkylation of N-acetyl-1,2-dihydroisoquinolines with diverse acceptor-acceptor diazo compounds has been achieved under a single catalytic system via metal carbene migratory insertion. Moreover, further synthetic transformations of the alkylated products such as aromatization, selective decarboxylation, and decarbonylation lead to the formation of several synthetically viable isoquinoline derivatives having immense potentials.
One-pot synthesis of β-O-4 lignin models: Via the insertion of stable 2-diazo-1,3-dicarbonyls into O-H bonds
Burtoloso, Antonio C. B.,De Oliveira, Gabriela P.,Dias, Rafael Mafra P.
, p. 4815 - 4823 (2020/07/13)
Because lignin is a macromolecule that is a sustainable source of aromatic compounds, model substrates are commonly used to increase our understanding of its complex structure. However, few methods have been described for the synthesis of these models. Herein, we describe a new route towards the synthesis of β-O-4 lignin models by intermolecular O-H insertion reactions with simple and stable diazocarbonyls. The benefits of this developed method were shorter reaction times and high yields, as well as mild and environmentally friendly conditions. This journal is
Addition of mixed (Alkenyl)dialkylzincates to vicinal diketo esters
Selter, Lars,Harms, Klaus,Koert, Ulrich
supporting information, p. 1215 - 1230 (2017/12/07)
Methods for the regioselective alkylation, arylation, and alkenylation of α,β-diketo esters using organozinc reagents are reported. Alkylation and arylation at the α-position is possi-ble using diorganozinc compounds. Alkenylation can be achieved using mixed (alkenyl)dineopentylzincates.
