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CAS 14123-60-5

3-Chlorophenylacetone TCI C2895

3-Chlorophenylacetone TCI C2895

Chemical Identity

Other names
1-(3-Chlorophenyl)-2-propanone
CAS No.
14123-60-5
PubChem
CID 2734097·SID 253661765
Formula
C9H9ClO
Molecular weight
168.62 g/mol
Purity
>95.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-(3-chlorophenyl)propan-2-one
SMILES
CC(=O)CC1=CC(=CC=C1)Cl
InChIKey
VCNYPJMEQHTAHS-UHFFFAOYSA-N
MDL
MDL00082872
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3-Chlorophenylacetone is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It plays a crucial role in laboratory settings where functional groups, such as ketone groups, are required for chemical reactions. Its versatility makes it an essential component in various synthetic pathways, enabling the creation of structurally diverse molecules. This compound is particularly valuable in research that demands precise chemical transformations and reactivity.

The compound's stable molecular structure and reactivity with a wide range of reagents make it a preferred choice for laboratory applications. It is easily involved in substitution and addition reactions, allowing for the synthesis of new compounds with varied structural features. Its availability in solid or liquid form enhances its usability across different experimental conditions. These properties make it a reliable and efficient reagent in organic chemistry laboratories.

In Indonesian laboratories, 3-Chlorophenylacetone is extensively used in organic chemistry research, especially in the synthesis of bioactive compounds. It is commonly found in studies related to pharmacological applications, including the development of pharmaceuticals and synthetic materials. Its role in creating compounds with potential therapeutic value underscores its importance in both academic and industrial research settings.

  • Organic synthesis of bioactive compounds due to its reactivity and structural versatility.
  • Development of pharmaceuticals through complex molecular transformations and functional group modifications.
  • Research in synthetic chemistry where ketone functionalities are essential for reaction pathways.
  • Creation of new chemical structures for industrial applications requiring tailored molecular properties.
  • Investigation of pharmacological agents through the synthesis of active pharmaceutical ingredients.

Brand TCI
CAS number 14123-60-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid or liquid, depending on supplier packaging
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

3-Chlorophenylacetone should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air. Due to its reactivity, it should be kept away from strong oxidizing agents and incompatible substances. Proper labeling and safe handling procedures are essential to ensure laboratory safety. Always follow standard chemical handling protocols to prevent accidental exposure. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications.

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