(S)-1-(tert-Butoxycarbonyl)-4,4-difluoro-2-methylpyrrolidine-2-carboxylic acid

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Reagent Code: #37940
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CAS Number 1194032-23-9

science Other reagents with same CAS 1194032-23-9

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Weight 265.2600 g/mol
Formula C₁₁H₁₇F₂NO₄
badge Registry Numbers
MDL Number MFCD22566252
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description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a 4,4-difluoro-2-methylpyrrolidine-2-carboxylic acid moiety, makes it valuable in the development of active pharmaceutical ingredients (APIs), particularly in the design of protease inhibitors and other biologically active compounds. The 4,4-difluoro group enhances metabolic stability and bioavailability, while the Boc group allows for selective deprotection during multi-step synthetic processes. It is often employed in peptide synthesis and medicinal chemistry to create novel drug candidates with improved efficacy and pharmacokinetic properties.

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inventory 50mg
10-20 days ฿8,118.00

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(S)-1-(tert-Butoxycarbonyl)-4,4-difluoro-2-methylpyrrolidine-2-carboxylic acid
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This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a 4,4-difluoro-2-methylpyrrolidine-2-carboxylic acid moiety, makes it valuable in the development of active pharmaceutical ingredients (APIs), particularly in the design of protease inhibitors and other biologically active compounds. The 4,4-difluoro group enhances metabolic stability

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a 4,4-difluoro-2-methylpyrrolidine-2-carboxylic acid moiety, makes it valuable in the development of active pharmaceutical ingredients (APIs), particularly in the design of protease inhibitors and other biologically active compounds. The 4,4-difluoro group enhances metabolic stability and bioavailability, while the Boc group allows for selective deprotection during multi-step synthetic processes. It is often employed in peptide synthesis and medicinal chemistry to create novel drug candidates with improved efficacy and pharmacokinetic properties.

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