65920-15-2 Usage
Uses
Used in Pharmaceutical Industry:
4-CHLORO-2-HYDROXYBENZOHYDRAZIDE is used as an intermediate in the manufacturing process for developing new pharmaceuticals, given its potential in creating effective therapeutic agents.
Used in Dye and Pigment Industry:
4-CHLORO-2-HYDROXYBENZOHYDRAZIDE is utilized as an intermediate in the production of dyes and pigments, contributing to the coloration and stability of these products.
Used in Organic Synthesis:
4-CHLORO-2-HYDROXYBENZOHYDRAZIDE is used as a reagent in the synthesis of various organic compounds, playing a crucial role in chemical reactions to form desired products.
Used in Antimicrobial and Antifungal Applications:
Due to its antimicrobial and antifungal properties, 4-CHLORO-2-HYDROXYBENZOHYDRAZIDE is used in the development of new therapeutic agents to combat infections and fungal growth.
Used in Antioxidant and Anti-inflammatory Research:
4-CHLORO-2-HYDROXYBENZOHYDRAZIDE is employed in research for its potential antioxidant and anti-inflammatory effects, which could lead to advancements in treatments for various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 65920-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,2 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65920-15:
(7*6)+(6*5)+(5*9)+(4*2)+(3*0)+(2*1)+(1*5)=132
132 % 10 = 2
So 65920-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7ClN2O2/c8-4-1-2-5(6(11)3-4)7(12)10-9/h1-3,11H,9H2,(H,10,12)
65920-15-2Relevant academic research and scientific papers
Identification and formation pathway of laccase-mediated oxidation products formed from hydroxyphenylureas
Jolivalt,Neuville,Boyer,Kerhoas,Mougin
, p. 5046 - 5054 (2007/10/03)
Hydroxyphenylureas are the first main metabolites formed in the environment from pesticide and biocide urea compounds. Because fungi release potent exocellular oxidases, we studied the ability of laccases produced by the white rot fungus, T. versicolor, to catalyze in vitro the transformation of five hydroxyphenylureas, to identify transformation pathways and mechanisms. Our results establish that the pH of the reaction has a strong influence on both the kinetics of the reaction and the nature of the transformation products. Structural characterization by spectroscopic methods (NMR, mass spectrometry) of eleven transformation products shows that laccase oxidizes the substrates to quinones or to polyaromatic oligomers. Slightly acidic conditions favor the formation of quinones as final transformation products. In contrast, at pH 5-6, the quinones further react with the remaining substrate in solution to give hetero-oligomers via carbon-carbon or carbon-oxygen bond formation. A reaction pathway is proposed for each of the identified products. These results demonstrate that fungal laccases could assist the transformation of hydroxyphenylureas.
