19893-72-2 Usage
Description
(4E)-5-[4-(dimethylamino)phenyl]-4-nitropent-4-en-1-yl acetate, also known as E-5-(4-dimethylaminophenyl)-4-nitropent-4-en-1-yl acetate, is a nitroalkene derivative with the molecular formula C16H20N2O4. It features a nitro group and a conjugated double bond, making it a significant intermediate in organic synthesis and medicinal chemistry research. This chemical compound is recognized for its potential biological activity and pharmacological properties, which are often the subject of scientific investigation.
Uses
Used in Organic Synthesis:
(4E)-5-[4-(dimethylamino)phenyl]-4-nitropent-4-en-1-yl acetate is used as a key intermediate in organic synthesis for the preparation of various organic compounds. Its unique structure and reactivity allow for the creation of a wide range of chemical products, contributing to the advancement of chemical research and development.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (4E)-5-[4-(dimethylamino)phenyl]-4-nitropent-4-en-1-yl acetate is utilized for its potential biological activity. Researchers explore its pharmacological properties to understand its possible applications in the development of new drugs and therapeutic agents.
Used in Pharmaceutical Development:
Due to its potential biological activity, (4E)-5-[4-(dimethylamino)phenyl]-4-nitropent-4-en-1-yl acetate is also used in pharmaceutical development. It may serve as a precursor or a building block in the synthesis of new pharmaceutical compounds, potentially leading to the discovery of novel treatments and medications.
Used in Chemical Research:
(4E)-5-[4-(dimethylamino)phenyl]-4-nitropent-4-en-1-yl acetate is employed in chemical research to study its reactivity and properties. Understanding how this compound interacts with other chemicals can provide insights into new reaction pathways and the development of innovative chemical processes.
Used in the Synthesis of Bioactive Compounds:
Given its potential biological activity, (4E)-5-[4-(dimethylamino)phenyl]-4-nitropent-4-en-1-yl acetate is used in the synthesis of bioactive compounds. This can lead to the creation of new molecules with specific biological functions, which may have applications in medicine, agriculture, and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19893-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,9 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19893-72:
(7*1)+(6*9)+(5*8)+(4*9)+(3*3)+(2*7)+(1*2)=162
162 % 10 = 2
So 19893-72-2 is a valid CAS Registry Number.
