92435-08-0 Usage
Chemical structure
A phenylurea derivative with a phenyl group and a chloroacetyl group attached to the nitrogen atoms
Pharmaceutical synthesis
Used in the synthesis of pharmaceuticals due to its versatile reactivity
Agrochemical synthesis
Utilized in the creation of agrochemicals
Anti-cancer potential
Studied for its potential as an anti-cancer agent
Enzyme inhibition
Investigated for its inhibitory effects on various enzymes
Building block
Shown promise as a building block for the synthesis of new compounds with potential therapeutic applications
Therapeutic applications
Explored for its potential in developing new treatments for various diseases and conditions
Check Digit Verification of cas no
The CAS Registry Mumber 92435-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,3 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92435-08:
(7*9)+(6*2)+(5*4)+(4*3)+(3*5)+(2*0)+(1*8)=130
130 % 10 = 0
So 92435-08-0 is a valid CAS Registry Number.
92435-08-0Relevant academic research and scientific papers
Synthesis, antimicrobial activities and molecular docking studies of novel 6-hydroxybenzofuran-3(2H)-one based 2,4-disubstituted 1,3-thiazoles
Lasczkowski, Krzysztof Z.,Misiura, Konrad,Biernasiuk, Anna,Malm, Anna,Siwek, Agata,Plech, Tomasz
, p. 798 - 807 (2013/12/04)
Synthesis, characterization and investigation of antibacterial and antifungal activities of thirteen novel 6-hydroxybenzofuran-3(2H)-one based 2,4-disubstituted 1,3-thiazoles are presented. Their structures were determined using NMR, FAB MS and HRMS analyses. The results of microbiological screening reveal that three derivatives containing fluorine, bromine and hydrogen substituents at the phenyl ring are the most active antimicrobial compounds. Molecular docking studies of all compounds on the active sites of microbial enzymes indicated a possible target N-myristoyltransferase (NMT). 2013 Bentham Science Publishers.
