N-(4-Phenylboronic)succinamic acid

95%

Reagent Code: #218564
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CAS Number 480424-95-1

science Other reagents with same CAS 480424-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.02 g/mol
Formula CH₁₂BNO₅
badge Registry Numbers
MDL Number MFCD03789260
thermostat Physical Properties
Melting Point 165 - 169 ℃
inventory_2 Storage & Handling
Density 1.37 g/cm3
Storage Room temperature

description Product Description

Used as a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical applications. The boronic acid functionality supports Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing complex molecules. Additionally, the boronic acid group allows reversible binding to diols, which is valuable in developing sensors for carbohydrates like glucose and in designing targeted therapies requiring specific molecular recognition. The succinamic acid moiety facilitates further derivatization and conjugation in the assembly of enzyme inhibitors and other bioactive compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,650.00
1g
10-20 days ฿9,310.00
N-(4-Phenylboronic)succinamic acid
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Used as a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical applications. The boronic acid functionality supports Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing complex molecules. Additionally, the boronic acid group allows reversible binding to diols, which is valuable in developing sensors for carbohydrates like glucose and in designing targeted therapies requiring specific molecular recognition. The suc

Used as a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical applications. The boronic acid functionality supports Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing complex molecules. Additionally, the boronic acid group allows reversible binding to diols, which is valuable in developing sensors for carbohydrates like glucose and in designing targeted therapies requiring specific molecular recognition. The succinamic acid moiety facilitates further derivatization and conjugation in the assembly of enzyme inhibitors and other bioactive compounds.

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