Methyl 3,4-Dihydroxy-2-methylbenzoate TCI M2713

Chemical Identity

CAS No.: 740799-82-0
PubChem: CID 59016598·SID 253660458
Formula: C9H10O4
Molecular weight: 182.17 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3,4-dihydroxy-2-methylbenzoate
SMILES: CC1=C(C=CC(=C1O)O)C(=O)OC
InChIKey: ONNFZKHTMFVKNY-UHFFFAOYSA-N

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Methyl 3,4-Dihydroxy-2-methylbenzoate is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. This building block plays a crucial role in constructing more complex molecular structures, particularly in the development of aromatic compounds and bioactive molecules. Its presence in various chemical reactions, such as oxidation, reduction, and substitution, makes it a valuable tool for researchers and students alike. Due to its structural stability and moderate reactivity, it can interact effectively with a range of reagents, enabling the creation of diverse chemical products.

The compound's unique molecular structure, featuring two hydroxyl groups and one methyl group, contributes to its reactivity and functional versatility. These functional groups allow it to participate in multiple chemical transformations, including esterification, hydrolysis, and reactions with alkali metals. This makes it an ideal candidate for applications in organic chemistry and biochemical research. Its ability to form ester derivatives and undergo hydrolytic reactions further enhances its utility in synthetic pathways.

In Indonesian laboratories, Methyl 3,4-Dihydroxy-2-methylbenzoate is commonly used by chemists and students for the synthesis of aromatic compounds and bioactive substances. Its availability and cost-effectiveness make it a popular choice for both educational and research purposes. Its role in supporting chemical experimentation aligns with the needs of local scientific communities, contributing to the advancement of chemical research in the region.

Related TCI products

Organic synthesis applications benefit from its structural versatility, allowing the creation of complex aromatic compounds and bioactive molecules.
It is suitable for esterification reactions due to its hydroxyl groups, which can form ester derivatives under appropriate conditions.
Hydrolysis reactions can be facilitated by its functional groups, making it useful in breaking down complex molecules into simpler components.
It supports substitution reactions, enabling the modification of molecular structures for various chemical applications.
Its reactivity with alkali metals makes it a valuable component in reactions requiring nucleophilic substitution and functional group transformations.

Brand	TCI
CAS number	740799-82-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid, crystalline
Storage	Store in a cool, dry place away from direct sunlight and moisture

Methyl 3,4-Dihydroxy-2-methylbenzoate should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its stability. The compound should be kept away from direct sunlight and sources of heat to avoid degradation. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during handling. Proper labeling of storage containers is also essential to prevent accidental exposure and ensure safe access. Regular inspection of storage conditions can help maintain the quality and usability of the compound for ongoing research and experimentation.

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