(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate

≥95%

Reagent Code: #232488
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CAS Number 220587-29-1

science Other reagents with same CAS 220587-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.29 g/mol
Formula C₂₁H₃₂BNO₆
badge Registry Numbers
MDL Number MFCD16251714
thermostat Physical Properties
Boiling Point 521.9±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.1 g/cm3
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of biologically active molecules, particularly in pharmaceutical development. Its primary application lies in Suzuki-Miyaura cross-coupling reactions, where the boronate ester group enables efficient carbon-carbon bond formation. This makes it valuable for constructing complex organic structures, especially in the production of chiral amino acid derivatives and peptidomimetics. The presence of the Boc-protected amine and ester functionalities allows for selective deprotection and further derivatization, supporting its use in multi-step syntheses of drug candidates. Commonly employed in research and development of protease inhibitors, receptor agonists, and other therapeutic agents requiring high enantiomeric purity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,490.00
1g
10-20 days ฿11,000.00
(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate
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Used as a key intermediate in the synthesis of biologically active molecules, particularly in pharmaceutical development. Its primary application lies in Suzuki-Miyaura cross-coupling reactions, where the boronate ester group enables efficient carbon-carbon bond formation. This makes it valuable for constructing complex organic structures, especially in the production of chiral amino acid derivatives and peptidomimetics. The presence of the Boc-protected amine and ester functionalities allows for selecti

Used as a key intermediate in the synthesis of biologically active molecules, particularly in pharmaceutical development. Its primary application lies in Suzuki-Miyaura cross-coupling reactions, where the boronate ester group enables efficient carbon-carbon bond formation. This makes it valuable for constructing complex organic structures, especially in the production of chiral amino acid derivatives and peptidomimetics. The presence of the Boc-protected amine and ester functionalities allows for selective deprotection and further derivatization, supporting its use in multi-step syntheses of drug candidates. Commonly employed in research and development of protease inhibitors, receptor agonists, and other therapeutic agents requiring high enantiomeric purity.

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