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TCI

CAS 16618-67-0

3-Bromo-5-nitroanisole TCI B4973

3-Bromo-5-nitroanisole TCI B4973

Chemical Identity

CAS No.
16618-67-0
PubChem
CID 12299076·SID 253661398
Formula
C7H6BrNO3
Molecular weight
232.03 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-bromo-3-methoxy-5-nitrobenzene
SMILES
COC1=CC(=CC(=C1)[N+](=O)[O-])Br
InChIKey
MEQKSFQEPDRNEQ-UHFFFAOYSA-N
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3-Bromo-5-nitroanisole is a chemical compound widely used as a building block in organic synthesis, playing a crucial role in laboratory research. This compound is commonly employed in various chemical reactions, particularly those involving electrophilic substitution or nitration processes. Its presence in laboratory settings is essential for the development of complex organic molecules, including heterocyclic compounds, pharmaceuticals, and industrial chemicals. Due to its structural versatility, it is a valuable resource for chemists seeking to explore new synthetic pathways.

The compound’s high reactivity is attributed to the presence of both bromo and nitro functional groups, which significantly influence its chemical behavior. These groups enhance its ability to participate in a wide range of reactions, making it a preferred choice for synthetic chemists. Its molecular structure allows for controlled reactivity under specific reaction conditions, offering flexibility in experimental design. The stability of the compound under controlled conditions further supports its reliability in laboratory applications.

In Indonesian laboratories, 3-Bromo-5-nitroanisole is frequently used in organic chemistry research, especially in pharmaceutical and industrial chemistry fields. It is also an essential teaching tool in higher education, where it helps students understand reactivity and complex synthesis techniques. Its application spans both research and educational settings, making it a fundamental compound in the chemical sciences.

  • Electrophilic substitution reactions benefit from the bromo group's ability to activate aromatic rings for substitution, enhancing synthetic versatility.
  • Nitration processes utilize the nitro group for introducing nitro functionality, critical in the synthesis of pharmaceuticals and dyes.
  • Heterocyclic compound synthesis relies on the compound's structural adaptability, enabling the creation of complex ring systems.
  • Educational experiments in organic chemistry use the compound to demonstrate reactivity and functional group behavior in controlled environments.
  • Industrial chemical production employs the compound as a key intermediate in the development of specialty chemicals and intermediates.

Brand TCI
CAS number 16618-67-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid crystalline powder
Storage Store in a cool, dry place away from light and incompatible substances

3-Bromo-5-nitroanisole should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be stored separately from strong oxidizing agents and incompatible materials. In laboratory settings, proper ventilation is essential to minimize exposure during handling. Always use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Regular inspection of storage conditions ensures the compound remains stable and safe for use in research and educational applications.

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