O-Acetyl-mandelic Acid Chloride

≥95%

Reagent Code: #59266
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CAS Number 1638-63-7

science Other reagents with same CAS 1638-63-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.62 g/mol
Formula C₁₀H₉ClO₃
badge Registry Numbers
MDL Number MFCD00000714
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in organic synthesis, it serves as a key intermediate for producing various pharmaceuticals, particularly those targeting neurological and cardiovascular conditions. Its reactivity makes it valuable in the formation of esters and amides, which are crucial in drug development. Additionally, it is employed in the preparation of chiral compounds, aiding in the creation of enantiomerically pure substances for therapeutic applications. Its role in peptide coupling reactions also highlights its importance in biochemical research and the production of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿12,591.00
inventory 5g
10-20 days ฿3,591.00
inventory 100g
10-20 days ฿35,991.00

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O-Acetyl-mandelic Acid Chloride
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Used primarily in organic synthesis, it serves as a key intermediate for producing various pharmaceuticals, particularly those targeting neurological and cardiovascular conditions. Its reactivity makes it valuable in the formation of esters and amides, which are crucial in drug development. Additionally, it is employed in the preparation of chiral compounds, aiding in the creation of enantiomerically pure substances for therapeutic applications. Its role in peptide coupling reactions also highlights its

Used primarily in organic synthesis, it serves as a key intermediate for producing various pharmaceuticals, particularly those targeting neurological and cardiovascular conditions. Its reactivity makes it valuable in the formation of esters and amides, which are crucial in drug development. Additionally, it is employed in the preparation of chiral compounds, aiding in the creation of enantiomerically pure substances for therapeutic applications. Its role in peptide coupling reactions also highlights its importance in biochemical research and the production of bioactive molecules.

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