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TCI

CAS 5847-59-6

2-Bromo-4-nitrophenol TCI B3918

2-Bromo-4-nitrophenol TCI B3918

Chemical Identity

CAS No.
5847-59-6
PubChem
CID 22109·SID 253659988
Formula
C6H4BrNO3
Molecular weight
218.00 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-bromo-4-nitrophenol
SMILES
C1=CC(=C(C=C1[N+](=O)[O-])Br)O
InChIKey
DCIPFSYBGTWYCR-UHFFFAOYSA-N
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2-Bromo-4-nitrophenol is a chemical compound widely used in laboratory settings as a foundational building block for various chemical reactions. It plays a crucial role in organic chemistry, particularly in the synthesis of aromatic and heterocyclic compounds. This compound is valued for its versatility and reactivity, making it an essential tool for researchers aiming to construct complex molecular structures. Its presence in chemical synthesis allows for the development of new materials and pharmaceuticals, contributing to the advancement of scientific research.

The compound's unique properties make it a preferred choice in laboratory applications. It features a phenolic structure with bromo and nitro substituents, which enhance its reactivity and polarity. The nitro group increases molecular polarity, while the bromo group contributes to electronic stability. These characteristics enable it to participate in a variety of reactions, including electrophilic substitution and nitration. Its relatively high melting and boiling points also facilitate isolation and purification processes, ensuring consistent results in experimental procedures.

In Indonesian laboratories, 2-Bromo-4-nitrophenol is commonly used in chemical research, including the synthesis of pharmaceutical compounds, polymers, and other organic materials. Its application spans across multiple scientific disciplines, supporting both academic and industrial research. As a key reagent, it is integral to the development of new chemical products and the exploration of molecular structures. Its reliability and chemical behavior make it a valuable resource for researchers in Indonesia.

  • Organic synthesis applications benefit from 2-Bromo-4-nitrophenol due to its reactivity and ability to participate in electrophilic substitution reactions.
  • Pharmaceutical research utilizes this compound for the development of new drug molecules, leveraging its structural versatility and functional groups.
  • Polymer science applications rely on its chemical properties to create advanced materials with specific functional characteristics.
  • Analytical chemistry experiments use it as a standard reference compound for spectroscopic and chromatographic analyses.
  • Environmental studies incorporate it to investigate the behavior of halogenated and nitro-substituted aromatic compounds in various matrices.

Brand TCI
CAS number 5847-59-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light and incompatible materials

2-Bromo-4-nitrophenol should be stored in a cool, dry environment, 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 chemicals. Laboratory personnel should handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to minimize exposure. Proper ventilation is essential when working with this material to ensure safe handling and reduce the risk of inhalation. Regular monitoring of storage conditions is advised to maintain the integrity and safety of the compound.

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