1-BOC-4-CYANO-4-(2-BROMOPHENYL)-PIPERIDINE

97%

Reagent Code: #149753
fingerprint
CAS Number 920023-51-4

science Other reagents with same CAS 920023-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.26 g/mol
Formula C₁₇H₂₁BrN₂O₂
thermostat Physical Properties
Boiling Point 468.9±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.35±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of centrally acting agents. Its structure supports the construction of complex piperidine-based molecules, which are common in neuroactive drugs. The BOC-protected amine, cyano group, and 2-bromophenyl substituent allow for selective reactions in multi-step organic syntheses, enabling diverse functionalizations such as cross-coupling. Commonly employed in research settings for creating analogs of antipsychotic or analgesic drugs. Not intended for direct therapeutic use.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 0.25g
10-20 days ฿6,480.00
inventory 1g
10-20 days ฿16,180.00
inventory 5g
10-20 days ฿52,290.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-BOC-4-CYANO-4-(2-BROMOPHENYL)-PIPERIDINE
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of centrally acting agents. Its structure supports the construction of complex piperidine-based molecules, which are common in neuroactive drugs. The BOC-protected amine, cyano group, and 2-bromophenyl substituent allow for selective reactions in multi-step organic syntheses, enabling diverse functionalizations such as cross-coupling. Commonly employed in research settings for creating analogs of antipsy

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of centrally acting agents. Its structure supports the construction of complex piperidine-based molecules, which are common in neuroactive drugs. The BOC-protected amine, cyano group, and 2-bromophenyl substituent allow for selective reactions in multi-step organic syntheses, enabling diverse functionalizations such as cross-coupling. Commonly employed in research settings for creating analogs of antipsychotic or analgesic drugs. Not intended for direct therapeutic use.

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...