(S)-2-((tert-Butoxycarbonyl)amino)propyl methanesulfonate

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Reagent Code: #236618
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CAS Number 126301-16-4

science Other reagents with same CAS 126301-16-4

blur_circular Chemical Specifications

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Weight 253.32 g/mol
Formula C₉H₁₉NO₅S
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MDL Number MFCD13188533
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of chiral pharmaceuticals, particularly in the preparation of optically active amino acid derivatives. It serves as a protected chiral building block in peptide chemistry, enabling selective alkylation reactions. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. Its sulfonate group allows for efficient nucleophilic substitution, facilitating the introduction of various functional groups in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,090.00
inventory 250mg
10-20 days ฿10,340.00
inventory 1g
10-20 days ฿27,890.00

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(S)-2-((tert-Butoxycarbonyl)amino)propyl methanesulfonate
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Used as an intermediate in the synthesis of chiral pharmaceuticals, particularly in the preparation of optically active amino acid derivatives. It serves as a protected chiral building block in peptide chemistry, enabling selective alkylation reactions. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. Its sulfonate group allows for efficient nucleophilic substitution, facilitating the introduction of various functional groups in

Used as an intermediate in the synthesis of chiral pharmaceuticals, particularly in the preparation of optically active amino acid derivatives. It serves as a protected chiral building block in peptide chemistry, enabling selective alkylation reactions. Commonly employed in the development of protease inhibitors and other bioactive molecules where stereochemistry is critical. Its sulfonate group allows for efficient nucleophilic substitution, facilitating the introduction of various functional groups in multi-step organic syntheses.

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