73023-89-9 Usage
Uses
Used in Pharmaceutical Research:
(E)-N,N-dimethyl-2-(5-nitrofuran-2-yl)ethenamine is used as an intermediate in the synthesis of various pharmaceutical compounds due to its unique structural features. Its presence in the structure can contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
(E)-N,N-dimethyl-2-(5-nitrofuran-2-yl)ethenamine serves as a building block in the creation of more complex organic molecules, which can be used in a wide range of applications, from pharmaceuticals to agrochemicals.
Used in Anti-infective and Antimicrobial Applications:
The presence of the nitro group in (E)-N,N-dimethyl-2-(5-nitrofuran-2-yl)ethenamine gives it potential as an anti-infective and antimicrobial agent. It can be used for developing new treatments against bacterial and fungal infections.
Used in Agrochemicals:
(E)-N,N-dimethyl-2-(5-nitrofuran-2-yl)ethenamine may also have applications in the agrochemical industry, where it could be used to develop new pesticides or fungicides to protect crops from diseases.
Used in Material Science:
(E)-N,N-dimethyl-2-(5-nitrofuran-2-yl)ethenamine's unique structure may also find use in the development of new materials with specific properties, such as improved stability or reactivity, which can be applied in various industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 73023-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,2 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73023-89:
(7*7)+(6*3)+(5*0)+(4*2)+(3*3)+(2*8)+(1*9)=109
109 % 10 = 9
So 73023-89-9 is a valid CAS Registry Number.
73023-89-9Relevant academic research and scientific papers
SYNTHESES OF 5-NITRO-2-FURYL- AND 5-NITRO-2-THIENYLACETONITRILES
Vegh, Daniel,Kovac, Jaroslav,Dandarova, Miloslava
, p. 114 - 117 (2007/10/02)
Syntheses of 5-niro-2-furyl- and 5-nitro-2-thienylacetonitriles have been accomplished by the reaction of enamines VIII with hydroxylamine-O-sulphonic acid and by nitration of furyl- and thienylacetontriles V.
