(R)-4-Boc-(3-Hydroxymethyl)morpholine

97%

Reagent Code: #230079
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CAS Number 215917-99-0

science Other reagents with same CAS 215917-99-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
thermostat Physical Properties
Boiling Point 320.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its free hydroxyl group and protected amine (Boc) functionality make it valuable in multi-step organic syntheses, especially in the preparation of kinase inhibitors and other bioactive molecules. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems due to its structural stability and compatibility with various coupling reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,510.00
5g
10-20 days ฿6,950.00
25g
10-20 days ฿31,990.00
100g
10-20 days ฿127,920.00
(R)-4-Boc-(3-Hydroxymethyl)morpholine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its free hydroxyl group and protected amine (Boc) functionality make it valuable in multi-step organic syntheses, especially in the preparation of kinase inhibitors and other bioactive molecules. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems due to its structural stability and compatibili

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its free hydroxyl group and protected amine (Boc) functionality make it valuable in multi-step organic syntheses, especially in the preparation of kinase inhibitors and other bioactive molecules. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems due to its structural stability and compatibility with various coupling reactions.

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