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CAS 24078-21-5

Methyl 3-Methyl-4-nitrobenzoate TCI M2145

Methyl 3-Methyl-4-nitrobenzoate TCI M2145

Chemical Identity

CAS No.
24078-21-5
PubChem
CID 260927·SID 125307789
Formula
C9H9NO4
Molecular weight
195.17 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 3-methyl-4-nitrobenzoate
SMILES
CC1=C(C=CC(=C1)C(=O)OC)[N+](=O)[O-]
InChIKey
IEFONJKJLZFGKQ-UHFFFAOYSA-N
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Methyl 3-Methyl-4-nitrobenzoate is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a key building block in the development of more complex organic molecules, making it an essential reagent for chemists. Its role in the laboratory extends to various synthetic pathways, including electrophilic substitution and reduction reactions. Due to its predictable chemical behavior and stability, it is a reliable choice for both academic and industrial research.

This compound is valued for its controlled reactivity and chemical stability, which allow it to participate in a wide range of reactions with reagents such as reducing agents, bases, and organic solvents. Its solubility in solvents like ethyl acetate and acetone further enhances its utility in laboratory applications. The compound’s non-mercurial and non-toxic nature under normal conditions ensures a safer working environment, making it a preferred option for researchers.

In Indonesian laboratories, Methyl 3-Methyl-4-nitrobenzoate is commonly used in organic chemistry research, particularly in university-level education and industrial applications. It plays a vital role in the synthesis of pharmaceutical compounds and industrial chemicals. Its availability in the local market supports research activities without the need for costly imports.

  • Organic synthesis reactions benefit from its role as a versatile building block for creating complex molecules.
  • Electrophilic substitution reactions utilize its stable structure for controlled chemical transformations.
  • Reduction reactions often employ this compound due to its predictable reactivity with reducing agents.
  • Pharmaceutical compound development relies on its use in the synthesis of active pharmaceutical ingredients.
  • Industrial chemical production incorporates it as a key intermediate in the manufacturing of specialty chemicals.

Brand TCI
CAS number 24078-21-5
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, crystalline appearance
Storage Store in a cool, dry place away from direct sunlight

Methyl 3-Methyl-4-nitrobenzoate 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 moisture absorption. The compound is non-mercurial and non-toxic under normal conditions, but standard laboratory safety practices should still be followed. It is advisable to store it away from incompatible substances such as strong acids or bases. Proper labeling and storage conditions ensure the compound remains safe and effective for use in research applications.

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