(2R,5S)-4-(Tert-Butoxycarbonyl)-5-Methylmorpholine-2-Carboxylic Acid

96%

Reagent Code: #231715
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CAS Number 1439319-94-4

science Other reagents with same CAS 1439319-94-4

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Weight 245.27 g/mol
Formula C₁₁H₁₉NO₅
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Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable for constructing enantiomerically pure compounds. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and conformational rigidity of the morpholine ring. Serves as an intermediate in the preparation of drug candidates targeting viral infections and metabolic disorders. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿27,450.00
inventory 250mg
10-20 days ฿46,660.00
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(2R,5S)-4-(Tert-Butoxycarbonyl)-5-Methylmorpholine-2-Carboxylic Acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable for constructing enantiomerically pure compounds. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and conformational rigidity of the morpholine ring. Serves as an intermediate in the preparation of drug candidates targeting viral infections and metabolic dis

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable for constructing enantiomerically pure compounds. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and conformational rigidity of the morpholine ring. Serves as an intermediate in the preparation of drug candidates targeting viral infections and metabolic disorders. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses.

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