(S)-3-Amino-2-methylbutan-2-olhydrochloride

95%

Reagent Code: #237437
fingerprint
CAS Number 168297-76-5

science Other reagents with same CAS 168297-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.62 g/mol
Formula C₅H₁₄ClNO
badge Registry Numbers
MDL Number MFCD16619112
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of bioactive molecules and active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its hydrochloride salt form enhances stability and solubility, making it suitable for use in multi-step organic reactions. Commonly employed in the development of antibiotics, enzyme inhibitors, and central nervous system agents due to its ability to influence the three-dimensional structure of drug candidates. Also utilized in asymmetric synthesis to introduce chirality, improving the selectivity and efficacy of therapeutic compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,550.00
inventory 1g
10-20 days ฿6,890.00
(S)-3-Amino-2-methylbutan-2-olhydrochloride
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of bioactive molecules and active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its hydrochloride salt form enhances stability and solubility, making it suitable for use in multi-step organic reactions. Commonly employed in the development of antibiotics, enzyme inhibitors, and central nervous system agents due to its ability to influence the three-dimensional structure of

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of bioactive molecules and active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its hydrochloride salt form enhances stability and solubility, making it suitable for use in multi-step organic reactions. Commonly employed in the development of antibiotics, enzyme inhibitors, and central nervous system agents due to its ability to influence the three-dimensional structure of drug candidates. Also utilized in asymmetric synthesis to introduce chirality, improving the selectivity and efficacy of therapeutic compounds.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...