6-Nitrobenzo[c][1,2]oxaborol-1(3H)-ol

95%

Reagent Code: #219381
label
Alias 2-hydroxymethyl-5-nitrophenylboronic acid half-ester
fingerprint
CAS Number 118803-40-0

science Other reagents with same CAS 118803-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.94 g/mol
Formula C₇H₆BNO₄
badge Registry Numbers
MDL Number MFCD04115657
thermostat Physical Properties
Boiling Point 330.6±52.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in medicinal chemistry as a key scaffold in the development of antibacterial and antifungal agents. The structure enables selective targeting of microbial enzymes due to its ability to mimic transition states in biochemical reactions. It is also explored in the design of boron-containing drugs for improved pharmacokinetics and binding affinity. Its nitro group enhances electron-withdrawing properties, supporting activity in bioactive molecules. Research applications include synthesis of inhibitors for bacterial leucyl-tRNA synthetase, making it relevant in combating resistant strains.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,320.00
inventory 250mg
10-20 days ฿3,930.00
inventory 5g
10-20 days ฿24,460.00
inventory 1g
10-20 days ฿7,760.00
6-Nitrobenzo[c][1,2]oxaborol-1(3H)-ol
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Used in medicinal chemistry as a key scaffold in the development of antibacterial and antifungal agents. The structure enables selective targeting of microbial enzymes due to its ability to mimic transition states in biochemical reactions. It is also explored in the design of boron-containing drugs for improved pharmacokinetics and binding affinity. Its nitro group enhances electron-withdrawing properties, supporting activity in bioactive molecules. Research applications include synthesis of inhibitors f

Used in medicinal chemistry as a key scaffold in the development of antibacterial and antifungal agents. The structure enables selective targeting of microbial enzymes due to its ability to mimic transition states in biochemical reactions. It is also explored in the design of boron-containing drugs for improved pharmacokinetics and binding affinity. Its nitro group enhances electron-withdrawing properties, supporting activity in bioactive molecules. Research applications include synthesis of inhibitors for bacterial leucyl-tRNA synthetase, making it relevant in combating resistant strains.

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