32337-96-5 Usage
Uses
Used in Organic Synthesis:
3-bromo-2-iodonitrobenzene is used as a substrate in various chemical reactions for the synthesis of complex organic molecules. Its unique structure, with both halogen and nitro groups, allows for versatile reactivity and functional group manipulation, making it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-bromo-2-iodonitrobenzene is used as a key intermediate in the synthesis of certain drugs. Its reactivity and the presence of halogens and the nitro group enable the creation of diverse molecular structures that can be further modified to develop new therapeutic agents.
Used in Agrochemical Industry:
3-bromo-2-iodonitrobenzene is also utilized in the agrochemical industry as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides. Its chemical properties allow for the development of compounds with specific modes of action, contributing to the control of pests and weeds in agriculture.
Used in Specialty Chemicals:
3-bromo-2-iodonitrobenzene is employed in the production of specialty chemicals, such as dyes, pigments, and polymers. Its unique structure and reactivity contribute to the development of novel materials with specific properties, such as color, stability, and reactivity, which are essential in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 32337-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,3 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32337-96:
(7*3)+(6*2)+(5*3)+(4*3)+(3*7)+(2*9)+(1*6)=105
105 % 10 = 5
So 32337-96-5 is a valid CAS Registry Number.
32337-96-5Relevant academic research and scientific papers
4 AND 5-Halo substituted 2-indanamine compounds
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, (2008/06/13)
2-Indanamine compounds having 4 and 5-halo substituents are inhibitors of phenylethanolamine N-methyltransferase.
