2-Amino-5-bromobenzonitrile
97%
Reagent
Code: #135198
CAS Number
39263-32-6
blur_circular Chemical Specifications
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Molecular Information
Weight
197.03 g/mol
Formula
C₇H₅BrN₂
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Registry Numbers
MDL Number
MFCD00158946
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Storage & Handling
Storage
Room temperature
description Product Description
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amino and nitrile functional groups, which readily undergo cyclization and substitution reactions. Commonly employed in the manufacture of agrochemicals, including certain herbicides and pesticides, where the bromine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. Also utilized in the production of dyes and fluorescent probes, benefiting from its aromatic structure and ability to participate in conjugated systems. Its versatility in organic synthesis makes it valuable in research and development within medicinal and industrial chemistry.
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2-Amino-5-bromobenzonitrile
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. It serves as a building block in the preparation of heterocyclic compounds due to the presence of both amino and nitrile functional groups, which readily undergo cyclization and substitution reactions. Commonly employed in the manufacture of agrochemicals, including certain herbicides and pesticides, where the bromine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. Also utilized in the production of dyes and fluorescent probes, benefiting from its aromatic structure and ability to participate in conjugated systems. Its versatility in organic synthesis makes it valuable in research and development within medicinal and industrial chemistry.
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