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TCI

CAS 2150-38-1

Methyl 3,4-Dimethoxybenzoate TCI M2805

Methyl 3,4-Dimethoxybenzoate TCI M2805

Chemical Identity

CAS No.
2150-38-1
PubChem
CID 16522·SID 354334045
Formula
C10H12O4
Molecular weight
196.20 g/mol
Purity
>98.0%(GC)
Reference databases
ChEBI·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 3,4-dimethoxybenzoate
SMILES
COC1=C(C=C(C=C1)C(=O)OC)OC
InChIKey
BIGQPYZPEWAPBG-UHFFFAOYSA-N
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Methyl 3,4-Dimethoxybenzoate is a chemical compound widely used in laboratory settings as a building block for the synthesis of complex organic molecules. This compound plays a crucial role in organic chemistry by serving as a versatile intermediate in various synthetic pathways. Its aromatic structure, combined with methoxy substituents, makes it an essential component in the development of more intricate chemical structures. In research environments, it is frequently employed to facilitate the creation of heterocyclic compounds and bioactive molecules.

The compound's chemical properties, including its stability and reactivity, make it a preferred choice for a wide range of experimental applications. It is non-polar and dissolves readily in organic solvents such as ethyl acetate and chloroform, which enhances its utility in reactions involving substitution or esterification. Its thermal stability allows it to remain effective under varying laboratory conditions, making it a reliable reagent for both routine and advanced chemical processes.

In Indonesian laboratories, Methyl 3,4-Dimethoxybenzoate is commonly used in academic and research institutions. It is a staple in chemical synthesis experiments, particularly in organic chemistry departments. Its availability and chemical versatility make it a go-to compound for researchers working on drug development, material science, and other advanced chemical studies. Its consistent performance and compatibility with standard laboratory procedures ensure its continued use in both teaching and research settings.

  • Organic synthesis of heterocyclic compounds due to its aromatic structure and methoxy substituents.
  • Esterification reactions because of its ability to participate in ester formation under appropriate conditions.
  • Substitution reactions in solvent systems like ethyl acetate and chloroform due to its solubility properties.
  • Bioactive molecule development as a precursor in the creation of compounds with pharmaceutical potential.
  • Teaching laboratory experiments to illustrate the principles of aromatic chemistry and functional group reactivity.

Brand TCI
CAS number 2150-38-1
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, crystalline appearance
Storage Store in a cool, dry place away from direct sunlight and moisture

Methyl 3,4-Dimethoxybenzoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its non-polar nature, it is best stored in glass or polyethylene containers that are resistant to organic solvents. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is not exposed to high temperatures or direct sunlight, as this may affect its chemical integrity. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental contamination.

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