21689-52-1 Usage
Description
(2Z)-3-amino-2-cyanoprop-2-enamide is an organic compound characterized by its molecular formula C4H6N2O. It features a linear structure with a Z-configuration around the double bond, and it incorporates both an amino group and a cyano group. (2Z)-3-amino-2-cyanoprop-2-enamide is recognized for its potential as a building block in the synthesis of complex organic and pharmaceutical molecules, as well as for its possible biological activities such as antiviral, antibacterial, and antifungal properties. Due to its reactivity and potential toxicity, it is essential to handle this compound with caution.
Uses
Used in Organic Synthesis:
(2Z)-3-amino-2-cyanoprop-2-enamide is utilized as a key intermediate in organic synthesis for the creation of various complex molecules. Its unique structure allows it to serve as a versatile building block, facilitating the development of new compounds with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2Z)-3-amino-2-cyanoprop-2-enamide is employed as a starting material for the development of new drugs. Its potential biological activities, such as antiviral, antibacterial, and antifungal properties, make it a promising candidate for the treatment of various infections and diseases.
Used in Antiviral Applications:
(2Z)-3-amino-2-cyanoprop-2-enamide is used as an antiviral agent, leveraging its potential to inhibit viral replication and reduce the severity of viral infections. This application is particularly relevant in the development of treatments for diseases caused by viruses.
Used in Antibacterial Applications:
(2Z)-3-amino-2-cyanoprop-2-enamide is also used as an antibacterial agent, where it can help combat bacterial infections by interfering with essential bacterial processes, thereby reducing the spread and severity of bacterial diseases.
Used in Antifungal Applications:
(2Z)-3-amino-2-cyanoprop-2-enamide is utilized in antifungal applications to treat fungal infections. Its ability to target and disrupt fungal cells makes it a valuable component in the development of antifungal medications.
Check Digit Verification of cas no
The CAS Registry Mumber 21689-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,8 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21689-52:
(7*2)+(6*1)+(5*6)+(4*8)+(3*9)+(2*5)+(1*2)=121
121 % 10 = 1
So 21689-52-1 is a valid CAS Registry Number.
