(S)-()-2-Chloromandelic acid

97%

Reagent Code: #234733
label
Alias (S)-2'-Chloro-α-hydroxyphenylacetic acid
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CAS Number 52950-19-3

science Other reagents with same CAS 52950-19-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.59 g/mol
Formula C₈H₇ClO₃
badge Registry Numbers
MDL Number MFCD00798437
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 anticoagulants and other bioactive molecules. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex organic reactions. Commonly employed in the development of α-hydroxy acids and as an intermediate in the preparation of optically active compounds for medicinal chemistry. Also utilized in the manufacture of agrochemicals and specialty polymers requiring specific stereochemical configurations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿242.00
inventory 25g
10-20 days ฿891.00
inventory 100g
10-20 days ฿5,320.00
inventory 500g
10-20 days ฿24,960.00
(S)-()-2-Chloromandelic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of anticoagulants and other bioactive molecules. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex organic reactions. Commonly employed in the development of α-hydroxy acids and as an intermediate in the preparation of optically active compounds for medicinal chemistry. Also utilized in the manufacture of agrochemicals and specialty polymer

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of anticoagulants and other bioactive molecules. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex organic reactions. Commonly employed in the development of α-hydroxy acids and as an intermediate in the preparation of optically active compounds for medicinal chemistry. Also utilized in the manufacture of agrochemicals and specialty polymers requiring specific stereochemical configurations.

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