4-(1,4-Dioxa-8-azaspiro[4.5]decan-8-ylsulfonyl)phenylboronic acid

98%

Reagent Code: #90319
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CAS Number 914610-70-1

science Other reagents with same CAS 914610-70-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.17 g/mol
Formula C₁₃H₁₈BNO₆S
badge Registry Numbers
MDL Number MFCD28384271
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling reactions are essential. Additionally, its unique spirocyclic structure can impart stability and specific reactivity, which is advantageous in designing novel compounds for medicinal chemistry. The compound is also explored in material science for creating advanced polymers and functional materials with tailored properties.

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inventory 1g
10-20 days ฿19,380.00

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4-(1,4-Dioxa-8-azaspiro[4.5]decan-8-ylsulfonyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling reactions are essential. Additionally, its unique spirocyclic structure can impart stability and specific reactivity, which is advantag
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling reactions are essential. Additionally, its unique spirocyclic structure can impart stability and specific reactivity, which is advantageous in designing novel compounds for medicinal chemistry. The compound is also explored in material science for creating advanced polymers and functional materials with tailored properties.
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