Methyl 2-(Chloromethyl)benzoate TCI M2203

Chemical Identity

CAS No.: 34040-62-5
PubChem: CID 118590·SID 125307647
Formula: C9H9ClO2
Molecular weight: 184.62 g/mol
Purity: >97.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 2-(chloromethyl)benzoate
SMILES: COC(=O)C1=CC=CC=C1CCl
InChIKey: AAHZCIWUDPKSJP-UHFFFAOYSA-N

Rp 4.213.650,00

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Methyl 2-(Chloromethyl)benzoate is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a versatile building block in chemical laboratories, particularly in the development of both heterocyclic and non-heterocyclic compounds. This reagent is commonly utilized in nucleophilic substitution and condensation reactions, making it a valuable asset for synthetic chemists. Its role in laboratory settings is critical for researchers aiming to create new compounds with specific functional groups and structural features.

The compound is favored for its stable chemical structure and controlled reactivity, which allow it to participate in a wide range of synthetic pathways without undergoing unwanted side reactions. It is soluble in organic solvents such as ethyl acetate and chloroform, which simplifies purification and isolation processes. These solubility properties make it an efficient choice for various experimental procedures, including chromatography and distillation. Its availability in different packaging options also supports its use across a broad spectrum of laboratory scales and applications.

In Indonesian laboratories, Methyl 2-(Chloromethyl)benzoate is frequently employed in organic chemistry research, especially in academic and research institutions. It is a key reagent for students and scientists working on the synthesis of complex organic molecules. Its cost-effective and reliable nature makes it a preferred choice for local research needs, supporting both educational and industrial applications in the chemical sector.

Related TCI products

Organic synthesis of heterocyclic compounds requiring chloromethyl functionality for ring formation and functional group introduction.
Preparation of intermediate compounds in pharmaceutical and agrochemical research due to its reactivity and solubility in organic solvents.
Nucleophilic substitution reactions where the chloromethyl group serves as a reactive site for further modification.
Condensation reactions in the synthesis of complex molecules with multiple functional groups.
Teaching and research applications in Indonesian universities and research institutes for training in synthetic chemistry techniques.

Brand	TCI
CAS number	34040-62-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various sizes to suit different laboratory needs
Physical form	Liquid
Storage	Store in a cool, dry place away from light and moisture

Methyl 2-(Chloromethyl)benzoate should be stored in a cool, dry place, away from direct light and moisture. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its organic nature, it should be kept in a well-ventilated area to minimize exposure. Avoid contact with incompatible materials such as strong bases or oxidizing agents. Always follow standard laboratory safety protocols when handling this compound, including the use of personal protective equipment. Proper storage ensures the compound remains stable and effective for use in chemical experiments.

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