93213-79-7 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(Bromomethyl)-3,4-Dichloro-1-Nitrobenzene is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into complex organic molecules, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 2-(Bromomethyl)-3,4-Dichloro-1-Nitrobenzene is employed as a precursor in the creation of pesticides and other crop protection agents, leveraging its chemical properties to enhance the effectiveness of these products.
Used in Dye and Pigment Manufacturing:
2-(Bromomethyl)-3,4-Dichloro-1-Nitrobenzene is utilized as an intermediate in the production of dyes and pigments, where its unique structure allows for the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing.
Safety Considerations:
Due to its hazardous nature, 2-(Bromomethyl)-3,4-Dichloro-1-Nitrobenzene should be handled with care to minimize its potential toxic and environmental impacts. Proper safety measures and disposal methods must be implemented to ensure the well-being of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 93213-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,1 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93213-79:
(7*9)+(6*3)+(5*2)+(4*1)+(3*3)+(2*7)+(1*9)=127
127 % 10 = 7
So 93213-79-7 is a valid CAS Registry Number.
93213-79-7Relevant academic research and scientific papers
Benzylic brominations with N-bromosuccinimide in (Trifluoromethyl)benzene
Suarez, Diana,Laval, Gilles,Tu, Shang-Min,Jiang, Dong,Robinson, Claire L.,Scott, Richard,Golding, Bernard T.
experimental part, p. 1807 - 1810 (2010/02/28)
A variety of benzylic brominations were performed by using N-bromosuccinimide in (trifluoromethyl)benzene with photochemical activation in the presence of 2,2′-azobisisobutyronitrile, 1,1′- azobis(cyclohexanecarbonitrile), or benzoyl peroxide as the radical initiator. This system provides clean, rapid, and high-yielding reactions with replacement of conventional solvents, such as tetrachloromethane, by less-toxic (trifluoromethyl)benzene. Georg Thieme Verlag Stuttgart.
