(S)-2-Cyclohexyl-2-hydroxyacetic acid

97%

Reagent Code: #237391
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CAS Number 61475-31-8

science Other reagents with same CAS 61475-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.19 g/mol
Formula C₈H₁₄O₃
badge Registry Numbers
MDL Number MFCD00057821
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds for drug manufacturing. Its stereochemistry makes it valuable in asymmetric synthesis, where it serves as a building block for active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Commonly applied in the production of central nervous system agents and enzyme inhibitors. Also utilized in research settings for developing novel organic molecules with targeted biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,120.00
inventory 250mg
10-20 days ฿5,270.00
inventory 1g
10-20 days ฿14,240.00
(S)-2-Cyclohexyl-2-hydroxyacetic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds for drug manufacturing. Its stereochemistry makes it valuable in asymmetric synthesis, where it serves as a building block for active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Commonly applied in the production of central nervous system agents and enzyme inhibitors. Also utilized in research settings for developing novel organic molecules with targeted biological activity

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds for drug manufacturing. Its stereochemistry makes it valuable in asymmetric synthesis, where it serves as a building block for active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Commonly applied in the production of central nervous system agents and enzyme inhibitors. Also utilized in research settings for developing novel organic molecules with targeted biological activity.

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