(S)-()-O-Acetylmandelic acid

98%

Reagent Code: #234734
label
Alias (S)-(+)-α-acetoxyphenylacetic acid
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CAS Number 7322-88-5

science Other reagents with same CAS 7322-88-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.19 g/mol
Formula C₁₀H₁₀O₄
badge Registry Numbers
MDL Number MFCD00064215
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of optically active drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex molecules. Commonly employed in the development of antibiotics, antivirals, and cardiovascular agents. Also utilized in the preparation of esters and amides as intermediates in fine chemical manufacturing. Its reactivity allows for easy introduction into larger molecular frameworks, making it a versatile intermediate in medicinal chemistry. Additionally, it serves as a resolving agent for separating optical isomers in drug development processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿174.00
inventory 25g
10-20 days ฿430.00
inventory 500g
10-20 days ฿6,690.00
inventory 100g
10-20 days ฿1,420.00
(S)-()-O-Acetylmandelic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of optically active drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex molecules. Commonly employed in the development of antibiotics, antivirals, and cardiovascular agents. Also utilized in the preparation of esters and amides as intermediates in fine chemical manufacturing. Its reactivity allows for easy introduction into larger mol

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of optically active drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex molecules. Commonly employed in the development of antibiotics, antivirals, and cardiovascular agents. Also utilized in the preparation of esters and amides as intermediates in fine chemical manufacturing. Its reactivity allows for easy introduction into larger molecular frameworks, making it a versatile intermediate in medicinal chemistry. Additionally, it serves as a resolving agent for separating optical isomers in drug development processes.

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