42867-31-2 Usage
Uses
Used in Organic Synthesis:
1-trityl-1H-pyrrole-2,5-dione is used as a key intermediate for the synthesis of various organic compounds due to its trityl-protected pyrrole-2,5-dione structure. This feature allows for selective reactions, enhancing the efficiency and specificity of organic synthesis processes.
Used in Pharmaceutical Industry:
1-trityl-1H-pyrrole-2,5-dione is utilized as a building block in the development of pharmaceuticals, contributing to the creation of novel drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1-trityl-1H-pyrrole-2,5-dione is employed as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides, to improve agricultural productivity and crop protection.
Used in Material Science:
1-trityl-1H-pyrrole-2,5-dione is used as a component in the synthesis of advanced materials, including polymers and composites, for applications in various industries, such as electronics, automotive, and aerospace.
Used as a Reagent in Chemical Industry:
1-trityl-1H-pyrrole-2,5-dione is used as a reagent in the preparation of pyrrole-2,5-dione derivatives, which are essential for a wide range of applications in the chemical industry, including the production of dyes, pigments, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 42867-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,6 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 42867-31:
(7*4)+(6*2)+(5*8)+(4*6)+(3*7)+(2*3)+(1*1)=132
132 % 10 = 2
So 42867-31-2 is a valid CAS Registry Number.
42867-31-2Relevant academic research and scientific papers
Intermediates in the synthesis of quinoline antibiotics
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, (2008/06/13)
This invention relates to compounds of the formulae STR1 wherein R and X are defined as below. These compounds are useful as intermediates in the syntheses of azabicyclo quinoline carboxylic acids having antibacterial activity.
