(3-((2,5-Dioxopyrrolidin-1-yl)methyl)phenyl)Vboronicacid

95%

Reagent Code: #180176
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CAS Number 950576-95-1

science Other reagents with same CAS 950576-95-1

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scatter_plot Molecular Information
Weight 233.03 g/mol
Formula C₁₁H₁₂BNO₄
badge Registry Numbers
MDL Number MFCD28167438
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and targeted cancer therapies. Its boronic acid functional group enables reversible interactions with biological targets such as enzymes, making it valuable in designing inhibitors for serine proteases. Commonly employed in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks found in bioactive molecules. Also utilized in the preparation of boron-containing drugs that benefit from enhanced binding affinity and metabolic stability. Its structure allows for further functionalization, supporting use in combinatorial chemistry and drug discovery research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,450.00
inventory 1g
10-20 days ฿12,000.00
inventory 5g
10-20 days ฿45,490.00

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(3-((2,5-Dioxopyrrolidin-1-yl)methyl)phenyl)Vboronicacid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and targeted cancer therapies. Its boronic acid functional group enables reversible interactions with biological targets such as enzymes, making it valuable in designing inhibitors for serine proteases. Commonly employed in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks found in bioactive molecules. Also utilized in the preparation of boron-containing dru

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and targeted cancer therapies. Its boronic acid functional group enables reversible interactions with biological targets such as enzymes, making it valuable in designing inhibitors for serine proteases. Commonly employed in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks found in bioactive molecules. Also utilized in the preparation of boron-containing drugs that benefit from enhanced binding affinity and metabolic stability. Its structure allows for further functionalization, supporting use in combinatorial chemistry and drug discovery research.

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