85325-83-3 Usage
Uses
Used in Organic Synthesis:
2,3-dimethoxy-6-nitrophenol is utilized as a key intermediate in organic synthesis, leveraging its functional groups to facilitate the creation of various chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,3-dimethoxy-6-nitrophenol serves as an intermediate for the production of certain medications, contributing to the development of new drugs and therapeutic agents.
Used in Dye and Pigment Manufacturing:
2,3-dimethoxy-6-nitrophenol is also employed as a starting material in the manufacturing of specific dyes and pigments, where its chemical structure is essential for achieving desired color properties.
Safety and Storage:
Due to its potential for skin and eye irritation, 2,3-dimethoxy-6-nitrophenol must be handled with care. It should be stored in a cool, dry place, away from incompatible materials to ensure safety and maintain its stability.
Check Digit Verification of cas no
The CAS Registry Mumber 85325-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,2 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85325-83:
(7*8)+(6*5)+(5*3)+(4*2)+(3*5)+(2*8)+(1*3)=143
143 % 10 = 3
So 85325-83-3 is a valid CAS Registry Number.
85325-83-3Relevant academic research and scientific papers
Liquid crystal compounds, mixtures and devices
-
Page column 28, (2008/06/13)
An electroclinic device having two spaced cell walls each bearing electrode structures and treated on at least one facing surface with an alignment layer, a layer of a smectic liquid crystal material enclosed between the cell walls, where the liquid crystal material contains one or more of the compounds described by formula I as defined in the specification.
Liquid crystal compounds, mixtures and devices
-
, (2008/06/13)
An electoclinic device having two spaced cell walls each bearing electrode structures and treated on at least one facing surface with an alignment layer, a layer of a smectic liquid crystal material enclosed between the cell walls, where the liquid crystal material contains one or more of the compounds described by formula I as defined in the specification.
The nitration of electron-rich aromatics
Dwyer,Holzapfel
, p. 7843 - 7848 (2007/10/03)
The successful mononitration of a variety of electron-rich aromatic substrates is reported, employing either nitronium tetrafluoroborate or 'claycop' as the nitrating agent. Dinitration of four of the substrates was achieved when employing nitronium tetrafluoroborate. Several of the products have previously been prepared only by indirect methods.
