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CAS 645-45-4

3-Phenylpropionyl Chloride TCI H0696

3-Phenylpropionyl Chloride TCI H0696

Chemical Identity

Other names
Hydrocinnamoyl Chloride
CAS No.
645-45-4
Formula
C9H9ClO
Molecular weight
168.62 g/mol
Purity
>97.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3-phenylpropanoyl chloride
SMILES
C1=CC=C(C=C1)CCC(=O)Cl
InChIKey
MFEILWXBDBCWKF-UHFFFAOYSA-N
MDL
MDL00000748
PubChem
CID 64801
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3-Phenylpropionyl Chloride 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 the modification of molecular structures is required. This reagent is particularly valuable in organic chemistry due to its ability to participate in various reactions, such as esterification and amide formation. Its reactivity makes it an essential tool for chemists aiming to construct more intricate chemical structures.

The compound is known for its stability and reactivity, especially toward bases and nucleophiles. Its solubility in organic solvents like ethyl acetate and chloroform facilitates efficient separation and reaction processes. These properties make it a preferred choice for substitution reactions and esterification processes. The compound’s versatility allows it to be applied in multiple synthetic pathways, enhancing its utility in both academic and industrial research.

In Indonesian laboratories, 3-Phenylpropionyl Chloride is commonly used in organic chemistry research, particularly in pharmaceutical and food chemistry fields. It is a key component in the development of new compounds with potential medical or industrial applications. Many research institutions and universities rely on this compound to advance their studies and create innovative chemical products.

  • Organic synthesis applications benefit from its reactivity and utility in building complex molecular structures.
  • Esterification reactions are enhanced by its solubility in organic solvents and its ability to form ester bonds.
  • Amide formation processes are supported by its role as a versatile acylating agent in synthetic pathways.
  • Pharmaceutical research utilizes it for the development of new drug compounds and molecular modifications.
  • Food chemistry studies employ it in the synthesis of flavor compounds and other organic derivatives.

Brand TCI
CAS number 645-45-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Liquid
Storage Store in a cool, dry place away from moisture and direct sunlight

3-Phenylpropionyl Chloride should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. The compound is corrosive and may cause irritation, so appropriate personal protective equipment should be worn when handling it. It should not be stored near incompatible materials such as strong bases or reactive metals. Regular monitoring of storage conditions ensures the compound remains stable and safe for use in laboratory applications.

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