(R)-3-Pyrrolidinemethanol

97%

Reagent Code: #229885
label
Alias D-beta-proline
fingerprint
CAS Number 110013-18-8

science Other reagents with same CAS 110013-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.15 g/mol
Formula C₅H₁₁NO
badge Registry Numbers
MDL Number MFCD09607969
thermostat Physical Properties
Boiling Point 176 °C
inventory_2 Storage & Handling
Density 0.978
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of neurologically active compounds, including agents targeting central nervous system disorders. Commonly employed in asymmetric synthesis due to its stereochemical stability and functional group compatibility. Also utilized in the preparation of catalysts and ligands for enantioselective reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿450.00
inventory 250mg
10-20 days ฿890.00
inventory 1g
10-20 days ฿2,020.00
inventory 5g
10-20 days ฿9,420.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-3-Pyrrolidinemethanol
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of neurologically active compounds, including agents targeting central nervous system disorders. Commonly employed in asymmetric synthesis due to its stereochemical stability and functional group compatibility. Also utilized in the preparation of catalysts and ligands for enantioselective

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of neurologically active compounds, including agents targeting central nervous system disorders. Commonly employed in asymmetric synthesis due to its stereochemical stability and functional group compatibility. Also utilized in the preparation of catalysts and ligands for enantioselective reactions.

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...