(R)-tert-Butyl 2-(chloromethyl)morpholine-4-carboxylate

95%

Reagent Code: #228577
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CAS Number 1260589-87-4

science Other reagents with same CAS 1260589-87-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.71 g/mol
Formula C₁₀H₁₈ClNO₃
thermostat Physical Properties
Boiling Point 313.1±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.132±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected morpholine ring and reactive chloromethyl group allow for selective functionalization, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in the preparation of kinase inhibitors and other targeted therapies. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,780.00
inventory 1g
10-20 days ฿44,760.00
(R)-tert-Butyl 2-(chloromethyl)morpholine-4-carboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected morpholine ring and reactive chloromethyl group allow for selective functionalization, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in the preparation of kinase inhibitors and other targeted therapies. Also utilized in asymmetric synthesis to introduce chirality in

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected morpholine ring and reactive chloromethyl group allow for selective functionalization, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in the preparation of kinase inhibitors and other targeted therapies. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

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