(S)-2-Hydroxy-3,3-dimethylbutanoic acid

95%

Reagent Code: #234906
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CAS Number 21641-92-9

science Other reagents with same CAS 21641-92-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 132.16 g/mol
Formula C₆H₁₂O₃
badge Registry Numbers
MDL Number MFCD00192212
thermostat Physical Properties
Melting Point 48-50°C
Boiling Point 242.4°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of certain pharmaceutical intermediates, particularly in the production of chiral compounds for drug development. Its stereochemistry makes it valuable in creating enantioselective molecules, especially in the development of antibiotics and other bioactive agents. Also employed as a building block in organic synthesis where a chiral hydroxy acid moiety is required. Its structural features allow for selective transformations in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,150.00
inventory 100mg
10-20 days ฿3,030.00
(S)-2-Hydroxy-3,3-dimethylbutanoic acid
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Used in the synthesis of certain pharmaceutical intermediates, particularly in the production of chiral compounds for drug development. Its stereochemistry makes it valuable in creating enantioselective molecules, especially in the development of antibiotics and other bioactive agents. Also employed as a building block in organic synthesis where a chiral hydroxy acid moiety is required. Its structural features allow for selective transformations in multi-step synthetic routes.

Used in the synthesis of certain pharmaceutical intermediates, particularly in the production of chiral compounds for drug development. Its stereochemistry makes it valuable in creating enantioselective molecules, especially in the development of antibiotics and other bioactive agents. Also employed as a building block in organic synthesis where a chiral hydroxy acid moiety is required. Its structural features allow for selective transformations in multi-step synthetic routes.

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