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CAS 14062-24-9

Ethyl 2-(4-Chlorophenyl)acetate TCI C3925

Ethyl 2-(4-Chlorophenyl)acetate TCI C3925

Chemical Identity

Other names
Ethyl (4-Chlorophenyl)acetate · 2-(4-Chlorophenyl)acetic Acid Ethyl Ester
CAS No.
14062-24-9
PubChem
CID 84177
Formula
C10H11ClO2
Molecular weight
198.65 g/mol
Purity
>98.0%(GC)
Storage
0-10°C
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
ethyl 2-(4-chlorophenyl)acetate
SMILES
CCOC(=O)CC1=CC=C(C=C1)Cl
InChIKey
UTWBWFXECVFDPZ-UHFFFAOYSA-N
MDL
MDL00018791
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Ethyl 2-(4-Chlorophenyl)acetate is a chemical compound widely used in organic synthesis reactions. It serves as a key building block in the production of aromatic compounds and their derivatives, particularly those containing phenyl and chloro groups. In the laboratory, it plays a crucial role in substitution reactions and esterification processes. Due to its complex molecular structure, it is also utilized in research to develop new compounds with specific properties. Its stability under certain conditions makes it a reliable material for chemical manipulation and experimentation.

This compound is preferred for its chemical stability and solubility in various organic solvents. It dissolves well in solvents such as ethyl acetate and ethanol, which facilitates its use in a wide range of chemical reactions. Its relatively high boiling point allows for controlled heating processes in laboratory settings. These properties make it a versatile and efficient reagent for both academic and industrial research applications.

In Indonesian laboratories, Ethyl 2-(4-Chlorophenyl)acetate is commonly used by researchers and students in higher education institutions and research organizations. It is particularly relevant in the study of organic chemistry, pharmaceutical development, and material science. Its availability and reliability make it an essential component in the chemical toolkit of Indonesian laboratories.

  • Organic synthesis reactions where phenyl and chloro groups are involved, due to its structural compatibility and reactivity.
  • Esterification processes as a versatile ester intermediate in the formation of various organic compounds.
  • Research in pharmaceutical development for the synthesis of drug-related compounds with specific functional groups.
  • Teaching and experimental work in university chemistry laboratories for student hands-on learning.
  • Industrial applications in the production of aromatic derivatives and specialty chemicals.

Brand TCI
CAS number 14062-24-9
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

Ethyl 2-(4-Chlorophenyl)acetate should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air. Due to its chemical nature, it should be handled in a well-ventilated area or fume hood to minimize inhalation risks. Avoid contact with skin and eyes, and use appropriate personal protective equipment when handling. Ensure that the storage area is secure and inaccessible to unauthorized personnel. Regular monitoring of storage conditions is advised to maintain the compound's stability and effectiveness in laboratory applications.

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