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TCI

CAS 104-21-2

4-Methoxybenzyl Acetate TCI A0886

4-Methoxybenzyl Acetate TCI A0886

Chemical Identity

CAS No.
104-21-2
PubChem
CID 7695·SID 87562396
Formula
C10H12O3
Molecular weight
180.20 g/mol
Purity
>98.0%(GC)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(4-methoxyphenyl)methyl acetate
SMILES
CC(=O)OCC1=CC=C(C=C1)OC
InChIKey
HFNGYHHRRMSKEU-UHFFFAOYSA-N
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4-Methoxybenzyl Acetate is a chemical compound widely used in synthetic reactions to produce complex compounds with aromatic structures. It serves as a key building block in organic chemistry, particularly in the synthesis of aromatic derivatives and related compounds. In laboratory settings, this compound plays a crucial role in various chemical processes, including substitution reactions and esterification. Its presence in chemical laboratories ensures the availability of essential materials for both research and educational purposes.

The compound's chemical properties make it a preferred choice for laboratory applications. It exhibits stability under normal conditions and can be easily decomposed when exposed to specific environmental factors. The presence of both a methoxy group and an ester group in its molecular structure contributes to its moderate reactivity, allowing it to participate in a wide range of chemical reactions without producing unwanted byproducts. These characteristics make it a reliable and versatile reagent for synthetic chemistry.

In Indonesian laboratories, 4-Methoxybenzyl Acetate is extensively used in organic chemistry research, particularly in the development of new compounds and the modification of existing ones. It is also commonly employed in educational settings to train students in synthesis techniques and chemical characterization methods. Its utility spans across both academic and industrial research environments, supporting a variety of chemical investigations.

  • Organic synthesis of aromatic derivatives due to its stable molecular structure and moderate reactivity.
  • Esterification reactions where the ester group facilitates the formation of new chemical bonds.
  • Substitution reactions in aromatic compounds, leveraging the methoxy group's electron-donating properties.
  • Educational experiments to demonstrate chemical reactivity and synthetic pathways in undergraduate chemistry courses.
  • Research applications in drug development and material science for the creation of complex organic molecules.

Brand TCI
CAS number 104-21-2
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

4-Methoxybenzyl Acetate should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to incompatible substances, and ensure proper ventilation in the laboratory environment. Regular monitoring of storage conditions is essential to maintain the compound's integrity and ensure safe usage in chemical experiments.

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