31739-63-6 Usage
Uses
Used in Pharmaceutical Research:
2-(1H-PYRROL-1-YL)BENZENE-1-CARBOHYDRAZIDE is used as a reactant in the preparation of various biologically active compounds, contributing to the development of new drugs and pharmaceuticals. Its structural properties allow it to be a building block in the synthesis of complex molecules, which can be utilized to create innovative therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, 2-(1H-PYRROL-1-YL)BENZENE-1-CARBOHYDRAZIDE serves as a key intermediate, facilitating the creation of a wide range of chemical products. Its reactivity and functional groups make it suitable for various synthetic pathways, enhancing the scope of organic compounds that can be produced.
Used in Materials Science Research:
2-(1H-PYRROL-1-YL)BENZENE-1-CARBOHYDRAZIDE may also have potential uses in research related to materials science, where its unique properties could be explored for the development of new materials with specific applications, such as in sensors, catalysts, or advanced materials with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 31739-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31739-63:
(7*3)+(6*1)+(5*7)+(4*3)+(3*9)+(2*6)+(1*3)=116
116 % 10 = 6
So 31739-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3O/c12-13-11(15)9-5-1-2-6-10(9)14-7-3-4-8-14/h1-8H,12H2,(H,13,15)
31739-63-6Relevant academic research and scientific papers
Inhibition of Copper-Dependent Amine Oxidases by Some Hydrazides of Pyrrol-1-ylbenzoic and Pyrrol-1-ylphenylacetic Acids
Artico, Marino,Corelli, Federico,Massa, Silvio,Stefancich, Giorgio,Avigliano, Luciana,et al.
, p. 802 - 806 (2007/10/02)
Some hydrazides of pyrrol-1-ylbenzoic and pyrrol-1-ylphenylacetic acids were prepared, and their effect on copper-dependent amine oxidases (Cu-AOs) and FAD monoamine oxidases (MAOs) activities was tested.The compounds were not substrates for Cu-AO enzymes
