(S)-2-((tert-Butoxycarbonyl)amino)-2-methylbutanoic acid

95%

Reagent Code: #234947
fingerprint
CAS Number 151171-11-8

science Other reagents with same CAS 151171-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
badge Registry Numbers
MDL Number MFCD12031697
thermostat Physical Properties
Boiling Point 341.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities make it ideal for solid-phase and solution-phase peptide synthesis. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its structural stability and defined stereoconfiguration. The tert-butoxycarbonyl (Boc) group allows for mild deprotection conditions, enabling selective and efficient multi-step synthetic routes in drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,600.00
inventory 250mg
10-20 days ฿16,000.00
(S)-2-((tert-Butoxycarbonyl)amino)-2-methylbutanoic acid
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities make it ideal for solid-phase and solution-phase peptide synthesis. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its structural stability and defined stereoconfiguration. The tert-butoxycarbonyl (Boc

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities make it ideal for solid-phase and solution-phase peptide synthesis. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its structural stability and defined stereoconfiguration. The tert-butoxycarbonyl (Boc) group allows for mild deprotection conditions, enabling selective and efficient multi-step synthetic routes in drug discovery and development.

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...