(S)-Methyl 4-((tert-butoxycarbonyl)amino)-2-(difluoromethoxy)butanoate

95%

Reagent Code: #236764
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CAS Number 1807916-70-6

science Other reagents with same CAS 1807916-70-6

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its (S)-stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. The Boc-protected amine and ester functionalities enable stepwise deprotection and coupling, useful in peptide-like chain elongation and multi-step drug manufacturing. The difluoromethoxy group enhances stability against enzymatic degradation and improves cell membrane permeability. Commonly applied in research and development of antiviral and anticancer agents.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,170.00
inventory 100mg
10-20 days ฿18,330.00
(S)-Methyl 4-((tert-butoxycarbonyl)amino)-2-(difluoromethoxy)butanoate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its (S)-stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. The Boc-protected amine and ester functionalities enable stepwise deprotection and coupling, useful in peptide-like chain elongation and multi-step drug manufacturing. The difluoromethoxy group enhances stabil
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its (S)-stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. The Boc-protected amine and ester functionalities enable stepwise deprotection and coupling, useful in peptide-like chain elongation and multi-step drug manufacturing. The difluoromethoxy group enhances stability against enzymatic degradation and improves cell membrane permeability. Commonly applied in research and development of antiviral and anticancer agents.
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