(R)-1-Ethylpiperidin-3-aminedihydrochloride

97%

Reagent Code: #231965
fingerprint
CAS Number 2031242-60-9

science Other reagents with same CAS 2031242-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.14 g/mol
Formula C₇H₁₈Cl₂N₂
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of central nervous system agents, including certain antipsychotics and antidepressants. The compound's chirality makes it valuable in asymmetric synthesis, where the (R)-enantiomer provides improved biological activity and selectivity. It is also employed in the preparation of novel receptor ligands for research in neuropharmacology. Due to its amine functionality protected as a salt, it offers better stability and handling in multi-step organic transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,500.00
inventory 1g
10-20 days ฿7,460.00
inventory 250mg
10-20 days ฿4,360.00
(R)-1-Ethylpiperidin-3-aminedihydrochloride
No image available

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of central nervous system agents, including certain antipsychotics and antidepressants. The compound's chirality makes it valuable in asymmetric synthesis, where the (R)-enantiomer provides improved biological activity and selectivity. It is also employed in the preparation of novel rece

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of central nervous system agents, including certain antipsychotics and antidepressants. The compound's chirality makes it valuable in asymmetric synthesis, where the (R)-enantiomer provides improved biological activity and selectivity. It is also employed in the preparation of novel receptor ligands for research in neuropharmacology. Due to its amine functionality protected as a salt, it offers better stability and handling in multi-step organic transformations.

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...