10077-97-1 Usage
Uses
Used in Pharmaceutical Applications:
Ethyl (1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)carbamate is used as a central nervous system depressant for its potential calming and sedative effects. It may be utilized in the development of medications targeting anxiety, insomnia, and other conditions that require CNS depression.
Used in Agricultural Applications:
In the agricultural industry, ethyl (1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)carbamate is used as a pesticide or herbicide. Its ability to inhibit the activity of certain enzymes makes it a potential candidate for controlling pests and unwanted plant growth, thereby enhancing crop protection and yield.
Further research is necessary to fully understand the properties and potential applications of ethyl (1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)carbamate, ensuring its safe and effective use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10077-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,7 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10077-97:
(7*1)+(6*0)+(5*0)+(4*7)+(3*7)+(2*9)+(1*7)=81
81 % 10 = 1
So 10077-97-1 is a valid CAS Registry Number.
10077-97-1Relevant articles and documents
Differential functional theory and molecular docking studies of newly synthesized carbamates
Danish, Muhammad,Raza, Muhammad A.,Anwar, Uzma,Rashid, Umer,Ahmed, Zaheer
, p. 1408 - 1415 (2019)
Four new carbamates (RZ1–RZ4) were synthesized from different amine moieties through reported methods. The reaction was monitored using thin layer chromatography and characterization was done using m.p., fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD) techniques. Density functional theory (DFT) studies were carried out using Gaussian 09 software to compare the theoretical and practical parameters of the synthesized compounds. Highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) were also drawn to calculate the energy difference between orbitals. In-vitro enzyme inhibition potential against acetylcholine esterase (AChE), butyrylcholine esterase (BChE), and protease was checked through standard protocols that suggested moderate inhibition against selected enzymes. Docking studies were also carried out, which depicted that these compounds have ability to bind on the active site of AChE and BChE.
