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CAS 7693-45-0

4-Chlorophenyl Chloroformate TCI C2545

4-Chlorophenyl Chloroformate TCI C2545

Chemical Identity

Other names
Chloroformic Acid 4-Chlorophenyl Ester
CAS No.
7693-45-0
PubChem
CID 139059·SID 172089041
Formula
C7H4Cl2O2
Molecular weight
191.01 g/mol
Purity
>98.0%(GC)(T)
Storage
0-10°C
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(4-chlorophenyl) carbonochloridate
SMILES
C1=CC(=CC=C1OC(=O)Cl)Cl
InChIKey
RYWGPCLTVXMMHO-UHFFFAOYSA-N
MDL
MDL00000638
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4-Chlorophenyl Chloroformate is a chemical compound widely used as a building block in organic synthesis. It is a versatile reagent that plays a key role in various laboratory processes, particularly in reactions involving esterification and carbonyl activation. This compound is derived from chloroformic acid and contains a chlorophenyl group, making it an essential component in the synthesis of complex organic molecules. Its reactivity and functional group compatibility make it a valuable tool for chemists working in both academic and industrial settings.

One of the main reasons this compound is preferred is its ability to react with a wide range of nucleophiles, including amines, hydroxides, and sulfides. This reactivity allows it to participate in substitution reactions and ester formation with high efficiency. Additionally, it maintains stability under controlled laboratory conditions, which simplifies its handling and storage. These properties make it a reliable choice for researchers seeking a consistent and effective reagent in their experiments.

In Indonesian laboratories, 4-Chlorophenyl Chloroformate is commonly used in organic chemistry research, especially in higher education institutions and research centers. It is a sought-after compound due to its role in synthesizing various organic compounds. Its availability and reliability make it a standard reagent in many chemical processes, supporting both teaching and research activities in the country.

  • Organic synthesis reactions benefit from its reactivity and ability to form esters efficiently.
  • Carbonyl activation processes rely on its capacity to activate carbon atoms for further chemical transformations.
  • Esterification reactions use this compound to create ester bonds with various functional groups.
  • Substitution reactions take advantage of its nucleophilic reactivity for molecular modification.
  • Research in chemical synthesis utilizes it as a key reagent for developing new compounds and materials.

Brand TCI
CAS number 7693-45-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid or liquid, depending on formulation
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances, and ensure proper disposal following laboratory safety guidelines. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use.

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