Methyl 4-Methoxy-3-nitrobenzoate TCI M2873

Chemical Identity

CAS No.: 40757-20-8
PubChem: CID 602104·SID 354334653
Formula: C9H9NO5
Molecular weight: 211.17 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 4-methoxy-3-nitrobenzoate
SMILES: COC1=C(C=C(C=C1)C(=O)OC)[N+](=O)[O-]
InChIKey: ZUZYMTBOKNSYEB-UHFFFAOYSA-N

Rp 610.050,00

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Methyl 4-Methoxy-3-nitrobenzoate is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a key building block for the development of more complex chemical structures. This compound is commonly found in chemical laboratories as a precursor for various synthetic pathways. Its versatility makes it an essential tool for researchers aiming to create new compounds with specific functional groups. Due to its chemical stability and reactivity, it is frequently employed in both substitution and reduction reactions.

The compound’s molecular structure features a nitro group and a methoxy group, contributing to its polarity and reactivity. These properties make it suitable for a range of chemical transformations, including nitro reduction to amines. Its polar nature also facilitates separation and isolation processes in chromatographic techniques. The presence of these functional groups enhances its utility in synthetic chemistry, particularly in the development of pharmaceutical and material science applications.

In Indonesian laboratories, Methyl 4-Methoxy-3-nitrobenzoate is commonly used in organic chemistry research, especially in the fields of pharmaceuticals and materials science. Local researchers often utilize this compound to synthesize new molecules with potential applications in medicine and industry. Its role in the synthesis of heterocyclic compounds and its use in chromatographic analysis make it a valuable resource for scientific studies in Indonesia.

Related TCI products

Synthesis of heterocyclic compounds for the development of new pharmaceuticals due to its reactivity and functional group versatility.
Nitro reduction reactions to produce amines, which are essential in the creation of complex organic molecules.
Chromatographic analysis for the separation and identification of compounds due to its polar nature and solubility properties.
Organic synthesis in material science research for the production of functional materials with specific chemical properties.
Development of new chemical entities in drug discovery programs requiring stable and reactive building blocks.

Brand	TCI
CAS number	40757-20-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from direct sunlight

Methyl 4-Methoxy-3-nitrobenzoate 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 sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize exposure to vapors. Avoid contact with incompatible materials such as strong acids or bases. Proper labeling and storage conditions ensure the compound remains stable and safe for use in laboratory settings.

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