(S)-1-(tert-Butoxycarbonyl)-4-oxopiperidine-2-carboxylic acid

95%

Reagent Code: #234975
fingerprint
CAS Number 198646-60-5

science Other reagents with same CAS 198646-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.26 g/mol
Formula C₁₁H₁₇NO₅
thermostat Physical Properties
Melting Point 121-125°C
Boiling Point 403.6°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 bioactive molecules and drug candidates targeting central nervous system disorders. Its structure features a Boc-protected piperidine ring with a ketone functional group at the 4-position and a carboxylic acid at the 2-position, enabling selective transformations in multi-step organic syntheses. Commonly employed in the preparation of piperidine-based protease inhibitors and receptor modulators. The Boc-protected amine allows for controlled deprotection, while the carboxylic acid facilitates coupling in peptide-like chains, making it valuable in medicinal chemistry for constructing complex, biologically active compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,450.00
1g
10-20 days ฿1,960.00
5g
10-20 days ฿8,060.00
25g
10-20 days ฿39,480.00
(S)-1-(tert-Butoxycarbonyl)-4-oxopiperidine-2-carboxylic acid
No image available
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure features a Boc-protected piperidine ring with a ketone functional group at the 4-position and a carboxylic acid at the 2-position, enabling selective transformations in multi-step organic syntheses. Commonly employed in the preparation of piperidine-based protease inhibitors and receptor modulators. The Boc-p
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure features a Boc-protected piperidine ring with a ketone functional group at the 4-position and a carboxylic acid at the 2-position, enabling selective transformations in multi-step organic syntheses. Commonly employed in the preparation of piperidine-based protease inhibitors and receptor modulators. The Boc-protected amine allows for controlled deprotection, while the carboxylic acid facilitates coupling in peptide-like chains, making it valuable in medicinal chemistry for constructing complex, biologically active 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...