[1-(6-Chloro-pyridin-3-ylmethyl)-piperidin-3-yl]-carbamicacidtert-butylester

97%

Reagent Code: #164250
fingerprint
CAS Number 939986-37-5

science Other reagents with same CAS 939986-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.834 g/mol
Formula C₁₆H₂₄ClN₃O₂
inventory_2 Storage & Handling
Density 1.19 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a key role in creating analogs for neurological research, including potential treatments for cognitive disorders, neuropathic pain, and depression. The tert-butyl carbamate group protects the amine during synthesis, allowing selective reactions at other sites, making it valuable in multi-step organic synthesis for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿19,750.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
[1-(6-Chloro-pyridin-3-ylmethyl)-piperidin-3-yl]-carbamicacidtert-butylester
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a key role in creating analogs for neurological research, including potential treatments for cognitive disorders, neuropathic pain, and depression. The tert-butyl carbamate group protects the amine during synthesis, allowing selective reactions at other sites, making it valuable in multi-step organic synthesis for drug discovery.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinic acetylcholine receptor modulators. It plays a key role in creating analogs for neurological research, including potential treatments for cognitive disorders, neuropathic pain, and depression. The tert-butyl carbamate group protects the amine during synthesis, allowing selective reactions at other sites, making it valuable in multi-step organic synthesis for drug discovery.

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...