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TCI

CAS 96-98-0

4-Methyl-3-nitrobenzoic Acid TCI M0950

4-Methyl-3-nitrobenzoic Acid TCI M0950

Chemical Identity

CAS No.
96-98-0
PubChem
CID 7319·SID 87572930
Formula
C8H7NO4
Molecular weight
181.15 g/mol
Purity
>99.0%(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-methyl-3-nitrobenzoic acid
SMILES
CC1=C(C=C(C=C1)C(=O)O)[N+](=O)[O-]
InChIKey
BBEWSMNRCUXQRF-UHFFFAOYSA-N
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4-Methyl-3-nitrobenzoic Acid is a chemical compound widely used in laboratory settings as a fundamental building block in organic synthesis. It plays a crucial role in the development of complex organic molecules, particularly in the field of aromatic chemistry. This compound is commonly found in chemical laboratories where it serves as a key component in the synthesis of aromatic derivatives and related compounds. Its unique molecular structure, featuring both a carboxylic acid group and a nitro group, makes it a versatile reagent in various chemical reactions.

The compound's high reactivity is due to its functional groups, which allow it to participate in a range of chemical transformations, including reduction, substitution, and aromatic reactions. Its chemical stability under controlled conditions makes it a reliable choice for laboratory use. However, it is sensitive to temperature and humidity, requiring careful handling and storage. The presence of the nitro group also contributes to its strong oxidizing properties, necessitating attention to safety during its use and storage.

In Indonesian laboratories, 4-Methyl-3-nitrobenzoic Acid is frequently utilized in organic chemistry research, especially in the synthesis of aromatic compounds and the development of pharmaceuticals. Its availability and affordability make it a popular choice among researchers and scientists working on complex chemical syntheses and drug discovery projects.

  • Organic synthesis of aromatic compounds due to its reactive functional groups and structural versatility.
  • Development of pharmaceutical intermediates through its participation in substitution and reduction reactions.
  • Research in chemical modification of aromatic derivatives for advanced material synthesis.
  • Investigation of oxidation reactions due to the presence of the nitro group.
  • Use in academic and industrial research settings for the creation of complex chemical structures.

Brand TCI
CAS number 96-98-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid, crystalline appearance
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its oxidizing properties, it should be handled with care, using appropriate personal protective equipment. Avoid storing near flammable materials. Ensure proper ventilation in the laboratory when working with this compound. Regular monitoring of storage conditions is essential to maintain its integrity and ensure safe laboratory practices.

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