Tert-butyl 4-(N-methoxy-N-methylcarbamoyl)piperidine-1-carboxylate

98%

Reagent Code: #240135
fingerprint
CAS Number 139290-70-3

science Other reagents with same CAS 139290-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.34 g/mol
Formula C₁₃H₂₄N₂O₄
badge Registry Numbers
MDL Number MFCD07368262
thermostat Physical Properties
Melting Point 71-75 °C
Boiling Point 343.8 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected piperidine derivative, enabling selective reactions at other functional sites in complex molecule assembly. Commonly applied in the development of bioactive molecules, including central nervous system agents and receptor modulators, due to the stability and ease of deprotection of the tert-butyl carbamate (Boc) group. The N-methoxy-N-methylcarbamoyl moiety allows for further transformation via reactions such as reductions or nucleophilic substitutions, making it valuable in medicinal chemistry for constructing drug-like scaffolds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,390.00
inventory 100g
10-20 days ฿5,250.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tert-butyl 4-(N-methoxy-N-methylcarbamoyl)piperidine-1-carboxylate
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected piperidine derivative, enabling selective reactions at other functional sites in complex molecule assembly. Commonly applied in the development of bioactive molecules, including central nervous system agents and receptor modulators, due to the stability and ease of deprotection of the tert-butyl carbamate (Boc) group. The N-methoxy-N-methylcarbamoyl moiety allows for further

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected piperidine derivative, enabling selective reactions at other functional sites in complex molecule assembly. Commonly applied in the development of bioactive molecules, including central nervous system agents and receptor modulators, due to the stability and ease of deprotection of the tert-butyl carbamate (Boc) group. The N-methoxy-N-methylcarbamoyl moiety allows for further transformation via reactions such as reductions or nucleophilic substitutions, making it valuable in medicinal chemistry for constructing drug-like scaffolds.

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...