(R)-(-)-N-BOC-3-pyrrolidinol

98%

Reagent Code: #229881
label
Alias (R)-1-Boc-3-hydroxypyrrolidine; (R)-1-(tert-butoxycarbonyl)-3-pyrrolidine alcohol
fingerprint
CAS Number 109431-87-0

science Other reagents with same CAS 109431-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₉H₁₇NO₃
badge Registry Numbers
MDL Number MFCD01317838
thermostat Physical Properties
Melting Point 62-65 °C(lit.)
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 active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities make it ideal for sequential coupling reactions in multi-step organic syntheses. Commonly employed in the production of neuroactive drugs, antivirals, and enzyme inhibitors where the (R)-enantiomer provides optimal biological activity. The BOC-protected amine allows for easy deprotection under mild acidic conditions, enabling further functionalization without racemization. Widely utilized in research and industrial settings for combinatorial chemistry and high-throughput screening of drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿174.00
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿330.00
inventory 25g
10-20 days ฿950.00
inventory 500g
10-20 days ฿16,530.00
inventory 100g
10-20 days ฿3,350.00
(R)-(-)-N-BOC-3-pyrrolidinol
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities make it ideal for sequential coupling reactions in multi-step organic syntheses. Commonly employed in the production of neuroactive drugs, antivirals, and enzyme inhibitors where the (R)-enantiomer provides optimal biological activity. The BOC-protected amine allows for easy deprot

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected alcohol and amine functionalities make it ideal for sequential coupling reactions in multi-step organic syntheses. Commonly employed in the production of neuroactive drugs, antivirals, and enzyme inhibitors where the (R)-enantiomer provides optimal biological activity. The BOC-protected amine allows for easy deprotection under mild acidic conditions, enabling further functionalization without racemization. Widely utilized in research and industrial settings for combinatorial chemistry and high-throughput screening of drug candidates.

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...