(3R)-1-ethylpiperidin-3-amine

97%

Reagent Code: #229083
fingerprint
CAS Number 1020396-26-2

science Other reagents with same CAS 1020396-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.2153 g/mol
Formula C₇H₁₆N₂
badge Registry Numbers
MDL Number MFCD19207947
thermostat Physical Properties
Boiling Point 155.1±8.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.898±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system (CNS) drugs. Its stereochemistry makes it valuable in developing enantioselective medications, including antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and selectivity toward neurotransmitter receptors. Also utilized in the development of radiolabeled derivatives for receptor imaging and pharmacokinetic studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,880.00
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿11,200.00
inventory 5g
10-20 days ฿48,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3R)-1-ethylpiperidin-3-amine
No image available

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system (CNS) drugs. Its stereochemistry makes it valuable in developing enantioselective medications, including antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and selectivity toward neurotransmitter receptors. Also utilized in the develop

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active ingredients for central nervous system (CNS) drugs. Its stereochemistry makes it valuable in developing enantioselective medications, including antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and selectivity toward neurotransmitter receptors. Also utilized in the development of radiolabeled derivatives for receptor imaging and pharmacokinetic studies.

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...