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CAS 99277-71-1

4-Bromo-2-nitrobenzoic Acid TCI B3810

4-Bromo-2-nitrobenzoic Acid TCI B3810

Chemical Identity

CAS No.
99277-71-1
PubChem
CID 3774467·SID 135727121
Formula
C7H4BrNO4
Molecular weight
246.01 g/mol
Purity
>98.0%(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-bromo-2-nitrobenzoic acid
SMILES
C1=CC(=C(C=C1Br)[N+](=O)[O-])C(=O)O
InChIKey
ZIRHHEZLJGORGU-UHFFFAOYSA-N
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4-Bromo-2-nitrobenzoic Acid is a versatile organic compound widely used in laboratory settings for its reactivity and structural versatility. As a key building block in synthetic chemistry, it plays a crucial role in the development of complex molecules across various scientific disciplines. This compound is commonly utilized in organic synthesis, where its functional groups enable the formation of a wide range of derivatives. Its presence in chemical laboratories makes it an essential reagent for researchers working on drug discovery, material science, and industrial chemistry applications.

The compound’s unique combination of bromo and nitro functional groups provides it with high reactivity and polarity, making it ideal for substitution reactions and electrophilic reactions. These properties allow chemists to manipulate its structure through various reaction mechanisms, leading to the synthesis of more complex and functional molecules. Its stability under controlled laboratory conditions ensures that it remains effective for extended periods, making it a reliable choice for both academic and industrial research.

In Indonesian laboratories, 4-Bromo-2-nitrobenzoic Acid is frequently used in organic chemistry research, particularly in the synthesis of aromatic compounds and bioactive molecules. It is also a common component in undergraduate and graduate chemistry practical courses, where students learn fundamental synthetic techniques. Its presence in educational and research institutions underscores its importance in advancing chemical knowledge and innovation in the region.

  • Organic synthesis of aromatic compounds due to its reactive bromo and nitro groups, enabling diverse functional group transformations.
  • Drug discovery and development as a building block for synthesizing bioactive molecules with pharmaceutical applications.
  • Material science research for creating functional polymers and advanced chemical materials with specific properties.
  • Educational use in chemistry laboratories to teach fundamental synthetic techniques and reaction mechanisms.
  • Industrial chemical production for the manufacture of specialty chemicals and intermediates in various manufacturing processes.

Brand TCI
CAS number 99277-71-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities as per supplier specifications
Physical form Solid powder
Storage Store in a cool, dry place away from direct sunlight and moisture

4-Bromo-2-nitrobenzoic Acid should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers made of glass or polyethylene to protect it from moisture and air exposure. Due to its reactivity, it should be handled in a well-ventilated area, ideally under a fume hood, to minimize exposure to vapors. Avoid contact with incompatible substances such as strong bases or reducing agents. Always wear appropriate personal protective equipment, including gloves, safety goggles, and a lab coat, when handling this compound to ensure safety in the laboratory environment.

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