trans-Cinnamoyl chloride

≥95%

Reagent Code: #159485
label
Alias Trans-3-phenylacryloyl chloride
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CAS Number 17082-09-6

science Other reagents with same CAS 17082-09-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.60 g/mol
Formula C₉H₇ClO
badge Registry Numbers
MDL Number MFCD00000732
thermostat Physical Properties
Melting Point 35 - 37 °C
Boiling Point 256 - 258 °C
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as an intermediate in organic synthesis, trans-Cinnamoyl chloride is key in the preparation of esters and amides for use in pharmaceuticals and agrochemicals. It reacts readily with alcohols and amines to form cinnamate esters and cinnamoyl amides, which exhibit biological activity such as antimicrobial and anti-inflammatory properties. It is also employed in the synthesis of fragrances and flavoring agents due to its aromatic structure. In research, it serves as a reagent for introducing the cinnamoyl group in complex molecules, aiding in the development of functional materials and bioactive compounds.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿300.00
inventory 100g
10-20 days ฿770.00
inventory 500g
10-20 days ฿3,470.00

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trans-Cinnamoyl chloride
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Used primarily as an intermediate in organic synthesis, trans-Cinnamoyl chloride is key in the preparation of esters and amides for use in pharmaceuticals and agrochemicals. It reacts readily with alcohols and amines to form cinnamate esters and cinnamoyl amides, which exhibit biological activity such as antimicrobial and anti-inflammatory properties. It is also employed in the synthesis of fragrances and flavoring agents due to its aromatic structure. In research, it serves as a reagent for introducing the
Used primarily as an intermediate in organic synthesis, trans-Cinnamoyl chloride is key in the preparation of esters and amides for use in pharmaceuticals and agrochemicals. It reacts readily with alcohols and amines to form cinnamate esters and cinnamoyl amides, which exhibit biological activity such as antimicrobial and anti-inflammatory properties. It is also employed in the synthesis of fragrances and flavoring agents due to its aromatic structure. In research, it serves as a reagent for introducing the cinnamoyl group in complex molecules, aiding in the development of functional materials and bioactive compounds.
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