3-Phenylpropionyl chloride

Standard for GC, ≥99.8%(GC)

Reagent Code: #222581
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CAS Number 645-45-4

science Other reagents with same CAS 645-45-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.62 g/mol
Formula C₉H₉ClO
badge Registry Numbers
EC Number 211-443-6
MDL Number MFCD00000748
thermostat Physical Properties
Melting Point -7-5 °C(lit.)
Boiling Point 107 °C/11 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.135 g/mL at 25 °C(lit.)
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for the preparation of active pharmaceutical ingredients. It reacts readily with amines to form amides, making it valuable in constructing peptide-like structures or drug scaffolds. Also employed in the synthesis of fragrances and flavoring agents due to its aromatic and ester-forming properties. Its reactivity allows for easy incorporation into more complex molecules, particularly in the development of anti-inflammatory and central nervous system agents. Commonly used in acylation reactions where a phenylpropionyl group needs to be introduced. As an acid chloride, it is highly reactive to moisture and should be handled in a dry, controlled environment.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,280.00
3-Phenylpropionyl chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for the preparation of active pharmaceutical ingredients. It reacts readily with amines to form amides, making it valuable in constructing peptide-like structures or drug scaffolds. Also employed in the synthesis of fragrances and flavoring agents due to its aromatic and ester-forming properties. Its reactivity allows for easy incorporation into more complex molecules, particularly in the development of anti

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for the preparation of active pharmaceutical ingredients. It reacts readily with amines to form amides, making it valuable in constructing peptide-like structures or drug scaffolds. Also employed in the synthesis of fragrances and flavoring agents due to its aromatic and ester-forming properties. Its reactivity allows for easy incorporation into more complex molecules, particularly in the development of anti-inflammatory and central nervous system agents. Commonly used in acylation reactions where a phenylpropionyl group needs to be introduced. As an acid chloride, it is highly reactive to moisture and should be handled in a dry, controlled environment.

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