(2S,6S)-2,6-Dimethylmorpholine

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Reagent Code: #70888
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CAS Number 276252-73-4

science Other reagents with same CAS 276252-73-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115.17 g/mol
Formula C₆H₁₃NO
badge Registry Numbers
MDL Number MFCD18250271
thermostat Physical Properties
Boiling Point 146.6±0.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

(2S,6S)-2,6-Dimethylmorpholine is primarily used as a chiral building block in the synthesis of various pharmaceutical compounds. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the production of active pharmaceutical ingredients (APIs) that require specific chiral configurations for efficacy. Additionally, it serves as a catalyst or ligand in asymmetric synthesis, enabling the creation of complex molecules with high stereoselectivity. In agrochemical research, it is employed to develop chiral pesticides and herbicides, enhancing their specificity and reducing environmental impact. Its applications also extend to the field of organic chemistry, where it is utilized in the preparation of fine chemicals and intermediates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿27,936.00
inventory 100mg
10-20 days ฿6,417.00
inventory 250mg
10-20 days ฿11,097.00

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(2S,6S)-2,6-Dimethylmorpholine
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(2S,6S)-2,6-Dimethylmorpholine is primarily used as a chiral building block in the synthesis of various pharmaceutical compounds. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the production of active pharmaceutical ingredients (APIs) that require specific chiral configurations for efficacy. Additionally, it serves as a catalyst or ligand in asymmetric synthesis, enabling the creation of complex molecules with high stereoselectivity. In agrochemi

(2S,6S)-2,6-Dimethylmorpholine is primarily used as a chiral building block in the synthesis of various pharmaceutical compounds. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the production of active pharmaceutical ingredients (APIs) that require specific chiral configurations for efficacy. Additionally, it serves as a catalyst or ligand in asymmetric synthesis, enabling the creation of complex molecules with high stereoselectivity. In agrochemical research, it is employed to develop chiral pesticides and herbicides, enhancing their specificity and reducing environmental impact. Its applications also extend to the field of organic chemistry, where it is utilized in the preparation of fine chemicals and intermediates.

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