R-()-1-Benzyl-3-pyrrolidinol

97%

Reagent Code: #71282
label
Alias (R)-1-Benzyl-3-pyrrolidinol, (R)-(+)-N-benzyl-3-hydroxypyrrolidine, (R)-1-benzyl-3-hydroxypyrrolidine
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CAS Number 101930-07-8

science Other reagents with same CAS 101930-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.24 g/mol
Formula C₁₁H₁₅NO
badge Registry Numbers
MDL Number MFCD00075484
thermostat Physical Properties
Boiling Point 116 °C0.9 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.07 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

R-()-1-Benzyl-3-pyrrolidinol is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the production of various pharmaceuticals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, which are crucial for developing drugs with specific therapeutic effects. The compound is often employed in the preparation of intermediates for active pharmaceutical ingredients (APIs), particularly in the creation of molecules that target neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it finds application in asymmetric catalysis, aiding in the production of complex organic molecules with high enantioselectivity. Its versatility and chiral nature make it a significant component in medicinal chemistry and drug discovery processes.

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Test Parameter Specification
Purity (GC) 97-100%
Refractive Index (n20D) 1.547-1.55
Specific Gravity (20°C) 1.071-1.074
A20 DC5 Methanol 2.8-4.8
Appearance Colorless to light yellow or brown liquid
Infrared Spectrum Conforms

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,920.00
inventory 5g
10-20 days ฿6,640.00
inventory 25g
10-20 days ฿20,280.00
inventory 100g
10-20 days ฿52,880.00

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R-()-1-Benzyl-3-pyrrolidinol
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R-()-1-Benzyl-3-pyrrolidinol is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the production of various pharmaceuticals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, which are crucial for developing drugs with specific therapeutic effects. The compound is often employed in the preparation of intermediates for active pharmaceutical ingredients (APIs), particularly in the creation of molecules that target neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it finds application in asymmetric catalysis, aiding in the production of complex organic molecules with high enantioselectivity. Its versatility and chiral nature make it a significant component in medicinal chemistry and drug discovery processes.
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