(S)-N-BOC-2-ETHYNYLPYRROLIDINE

95%

Reagent Code: #238020
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CAS Number 130495-08-8

science Other reagents with same CAS 130495-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.26 g/mol
Formula C₁₁H₁₇NO₂
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MDL Number MFCD10698161
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neurologically active compounds. Its protected amine group and alkyne functionality allow for selective reactions in multi-step organic syntheses. The ethynyl group enables click chemistry applications, such as Huisgen cycloaddition, useful in drug discovery and bioconjugation. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to its rigid pyrrolidine scaffold and stereochemical purity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,700.00
inventory 5g
10-20 days ฿14,100.00
(S)-N-BOC-2-ETHYNYLPYRROLIDINE
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neurologically active compounds. Its protected amine group and alkyne functionality allow for selective reactions in multi-step organic syntheses. The ethynyl group enables click chemistry applications, such as Huisgen cycloaddition, useful in drug discovery and bioconjugation. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to its rigid pyrrolidine sca

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neurologically active compounds. Its protected amine group and alkyne functionality allow for selective reactions in multi-step organic syntheses. The ethynyl group enables click chemistry applications, such as Huisgen cycloaddition, useful in drug discovery and bioconjugation. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to its rigid pyrrolidine scaffold and stereochemical purity.

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