31431-23-9 Usage
Uses
Used in Organic Synthesis:
(4-amino-3-nitrophenyl) cyclopropyl ketone is used as a key intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-amino-3-nitrophenyl) cyclopropyl ketone is utilized as a building block for the development of novel drugs, targeting a range of therapeutic areas.
Used in Dye and Pigment Production:
(4-amino-3-nitrophenyl) cyclopropyl ketone is also employed as an intermediate in the production of dyes and pigments, highlighting its versatility in different chemical applications.
Used in Biological and Pharmacological Studies:
(4-amino-3-nitrophenyl) cyclopropyl ketone has been studied for its potential biological and pharmacological properties, including its anti-inflammatory and anti-cancer activities, which could lead to the development of new therapeutic agents for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 31431-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,3 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31431-23:
(7*3)+(6*1)+(5*4)+(4*3)+(3*1)+(2*2)+(1*3)=69
69 % 10 = 9
So 31431-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O3/c11-8-4-3-7(5-9(8)12(14)15)10(13)6-1-2-6/h3-6H,1-2,11H2
31431-23-9Relevant academic research and scientific papers
Synthesis and anthelminthic acitivity of alkyl-(5-acyl-1-benzimidazol-2-yl) carbamates
Raeymackers,Van Gelder,Roevens,Janssen
, p. 586 - 594 (2007/10/05)
A series of alkyl-(5-acyl-l-H-benzimidazol-2-yl)-carbamates were prepared and screened for anthelminthic activity. Some of them were found to be fully active at low, atoxic oral dose levels against gastro-intestinal nematodes. The activity against Syphacia muris and Strongyloides ratta is indicated. From these studies methyl (5-benzoyl-1-H-benzimidazol-2-yl) carbamate (mebendazole) and methyl [5-(4-fluorobenzoyl)-1-H-benzimidazol-2-yl]carbamate (flubendazole) were selected for detailed investigation.
