TERT-BUTYL 4-AMINO-2-METHYLPIPERIDINE-1-CARBOXYLATE

95%

Reagent Code: #244896
fingerprint
CAS Number 952182-04-6

science Other reagents with same CAS 952182-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD09832897
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require a protected amine functional group. Its piperidine backbone with a tert-butoxycarbonyl (Boc) protecting group makes it valuable in multi-step organic syntheses, especially for drugs targeting central nervous system disorders, metabolic diseases, and certain oncology treatments. The compound allows for selective reactions at the amino site after deprotection, enabling precise construction of complex drug molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemistry and stability under various reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿25,080.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
TERT-BUTYL 4-AMINO-2-METHYLPIPERIDINE-1-CARBOXYLATE
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require a protected amine functional group. Its piperidine backbone with a tert-butoxycarbonyl (Boc) protecting group makes it valuable in multi-step organic syntheses, especially for drugs targeting central nervous system disorders, metabolic diseases, and certain oncology treatments. The compound allows for selective reactions at the amino site after dep

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that require a protected amine functional group. Its piperidine backbone with a tert-butoxycarbonyl (Boc) protecting group makes it valuable in multi-step organic syntheses, especially for drugs targeting central nervous system disorders, metabolic diseases, and certain oncology treatments. The compound allows for selective reactions at the amino site after deprotection, enabling precise construction of complex drug molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemistry and stability under various reaction conditions.

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...