Oxolane-2-carbonyl chloride

95%

Reagent Code: #222008
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CAS Number 52449-98-6

science Other reagents with same CAS 52449-98-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.56 g/mol
Formula C₅H₇ClO₂
badge Registry Numbers
MDL Number MFCD09897727
inventory_2 Storage & Handling
Storage 2-8℃, inert gas storage

description Product Description

Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to form amide and ester derivatives, making it useful in constructing complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where a five-membered cyclic ether-derived moiety is required. Additionally, it serves in peptide coupling reactions and the development of specialty polymers due to its ability to introduce functionalized cyclic structures. Its role as a derivatizing agent also extends to analytical chemistry for modifying carboxylic acids and alcohols in sample preparation.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,120.00
250mg
10-20 days ฿4,670.00
1g
10-20 days ฿11,660.00
Oxolane-2-carbonyl chloride
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Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to form amide and ester derivatives, making it useful in constructing complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where a five-membered cyclic ether-derived moiety is required. Additionally, it serves in peptide coupling reactions and the development of specialty polym

Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to form amide and ester derivatives, making it useful in constructing complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where a five-membered cyclic ether-derived moiety is required. Additionally, it serves in peptide coupling reactions and the development of specialty polymers due to its ability to introduce functionalized cyclic structures. Its role as a derivatizing agent also extends to analytical chemistry for modifying carboxylic acids and alcohols in sample preparation.

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