(R)tert-Butoxycarbonylamino-(3-chloro-phenyl)-aceticacid

>97%

Reagent Code: #230231
fingerprint
CAS Number 926641-28-3

science Other reagents with same CAS 926641-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.72 g/mol
Formula C₁₃H₁₆ClNO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure allows for selective reactions in peptide-like chains, making it valuable in creating amino acid derivatives. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in protease inhibitors and receptor modulators. The Boc-protected amine group enables controlled deprotection during multi-step syntheses, ensuring compatibility with various reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,680.00
inventory 250mg
10-20 days ฿2,220.00
inventory 1g
10-20 days ฿5,290.00
(R)tert-Butoxycarbonylamino-(3-chloro-phenyl)-aceticacid
No image available
Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure allows for selective reactions in peptide-like chains, making it valuable in creating amino acid derivatives. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in protease inhibitors and receptor modulators. The Boc-protected amine group enables controlled deprotection
Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure allows for selective reactions in peptide-like chains, making it valuable in creating amino acid derivatives. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in protease inhibitors and receptor modulators. The Boc-protected amine group enables controlled deprotection during multi-step syntheses, ensuring compatibility with various reaction conditions.
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...