4-Amino-3-nitrophenylboronicacid

98%

Reagent Code: #137333
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CAS Number 89466-07-9

science Other reagents with same CAS 89466-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.94 g/mol
Formula C₆H₇BN₂O₄
badge Registry Numbers
MDL Number MFCD07437851
thermostat Physical Properties
Melting Point 215 - 225 ℃
Boiling Point 439.5 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.48 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Also employed in the preparation of sensors and probes for detecting biologically relevant molecules due to the reactivity of the boronic acid group with diols and amines. The presence of both amino and nitro groups allows for further functionalization, supporting its use in multi-step organic syntheses and library generation for drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,460.00
250mg
10-20 days ฿4,260.00
1g
10-20 days ฿12,220.00
4-Amino-3-nitrophenylboronicacid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Also employed in the preparation of sensors and probes for detecting biologically relevant molecules due to the reactivity of the boronic acid group with diols and amines. The

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Also employed in the preparation of sensors and probes for detecting biologically relevant molecules due to the reactivity of the boronic acid group with diols and amines. The presence of both amino and nitro groups allows for further functionalization, supporting its use in multi-step organic syntheses and library generation for drug discovery.

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