(S)-Tert-Butyl 4,5-Diamino-5-Oxopentanoate

97%

Reagent Code: #237123
fingerprint
CAS Number 17193-29-2

science Other reagents with same CAS 17193-29-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.25 g/mol
Formula C₉H₁₈N₂O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs and enzyme inhibitors. The tert-butyl ester protects the carboxylate group, enabling selective reactions at the amine groups in multi-step organic syntheses. Commonly employed in the preparation of beta-amino acids and other bioactive molecules where stereochemistry plays a critical role in biological activity. Also utilized in the production of specialty polymers and ligands for asymmetric catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,760.00
inventory 1g
10-20 days ฿22,530.00
inventory 5g
10-20 days ฿60,420.00
inventory 250mg
10-20 days ฿11,280.00
(S)-Tert-Butyl 4,5-Diamino-5-Oxopentanoate
No image available

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs and enzyme inhibitors. The tert-butyl ester protects the carboxylate group, enabling selective reactions at the amine groups in multi-step organic syntheses. Commonly employed in the preparation of beta-amino acids and other bioactive molecules where stereochemistry plays a critical role in biological activity. Also utilized in the production of specialty polymers and l

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs and enzyme inhibitors. The tert-butyl ester protects the carboxylate group, enabling selective reactions at the amine groups in multi-step organic syntheses. Commonly employed in the preparation of beta-amino acids and other bioactive molecules where stereochemistry plays a critical role in biological activity. Also utilized in the production of specialty polymers and ligands for asymmetric catalysis.

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...