1-Piperidinecarboxylicacid, 4-hydroxy-4-methyl-, phenylmethyl ester

97%

Reagent Code: #222681
fingerprint
CAS Number 169750-57-6

science Other reagents with same CAS 169750-57-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.3056 g/mol
Formula C₁₄H₁₉NO₃
badge Registry Numbers
MDL Number MFCD09910308
thermostat Physical Properties
Boiling Point 383.9±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.180±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals. It serves as a protected form of 4-hydroxy-4-methylpiperidine, enabling controlled reactions in multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) where selective functional group manipulation is required. Its benzyl ester group allows for easy deprotection under mild conditions, making it valuable in peptide and heterocyclic chemistry. Also utilized in the production of agrochemicals and specialty polymers due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,840.00
inventory 500mg
10-20 days ฿6,200.00
1-Piperidinecarboxylicacid, 4-hydroxy-4-methyl-, phenylmethyl ester
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals. It serves as a protected form of 4-hydroxy-4-methylpiperidine, enabling controlled reactions in multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) where selective functional group manipulation is required. Its benzyl ester group allows for easy deprotection under mild conditions, making it valuable in peptide and heterocyclic chemistry. Also utilized in the

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals. It serves as a protected form of 4-hydroxy-4-methylpiperidine, enabling controlled reactions in multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) where selective functional group manipulation is required. Its benzyl ester group allows for easy deprotection under mild conditions, making it valuable in peptide and heterocyclic chemistry. Also utilized in the production of agrochemicals and specialty polymers due to its stability and reactivity profile.

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...