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TCI

CAS 53088-68-9

Methyl (3-Chlorophenyl)acetate TCI M2142

Methyl (3-Chlorophenyl)acetate TCI M2142

Chemical Identity

CAS No.
53088-68-9
PubChem
CID 2733544·SID 125307788
Formula
C9H9ClO2
Molecular weight
184.62 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 2-(3-chlorophenyl)acetate
SMILES
COC(=O)CC1=CC(=CC=C1)Cl
InChIKey
HTBBVKFFDDQVER-UHFFFAOYSA-N
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Methyl (3-Chlorophenyl)acetate is a chemical compound widely used as a building block in organic synthesis. It plays a crucial role in laboratories by enabling the creation of complex organic molecules, particularly those involving aromatic structures and ester functionalities. This compound is valued for its versatility and stability, making it an essential tool for researchers in various scientific disciplines. Its ability to participate in multiple chemical reactions, such as hydrolysis and esterification, enhances its utility in synthetic pathways.

The compound’s chemical properties, including its stability and reactivity in controlled environments, make it a preferred choice for synthetic chemists. It is compatible with both organic solvents and aqueous solutions, offering flexibility in reaction conditions. Its non-reactive nature also simplifies purification and isolation processes, reducing the complexity of laboratory workflows. These characteristics contribute to its widespread use in both academic and industrial research settings.

In Indonesian laboratories, Methyl (3-Chlorophenyl)acetate is commonly used in chemical research and development. It is a key component in the synthesis of pharmaceuticals, materials, and specialty chemicals. Its availability and reliability make it a standard reagent in both teaching and research laboratories across Indonesia. Its role in advancing scientific discovery is well recognized in the local scientific community.

  • Organic synthesis for creating aromatic and ester-based compounds due to its structural versatility and reactivity.
  • Pharmaceutical research for developing new drug molecules that require ester functionalities in their structure.
  • Material science applications in the production of polymers and specialty chemicals requiring functional group modification.
  • Teaching laboratories for demonstrating esterification and hydrolysis reactions in undergraduate chemistry courses.
  • Industrial research for the development of fine chemicals and intermediates in the chemical manufacturing sector.

Brand TCI
CAS number 53088-68-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard chemical supply practices
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

Methyl (3-Chlorophenyl)acetate 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 potential reactivity under certain conditions, it should be stored away from strong oxidizing agents and incompatible substances. Appropriate personal protective equipment, such as gloves and safety goggles, should be worn when handling the compound. Regular monitoring of storage conditions is advised to ensure the integrity of the material. Proper labeling of containers is essential for safe handling and to prevent accidental misuse in the laboratory.

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