2-(Methylsulfinyl)benzeneboronic acid, 97%, Thermo Scientific Chemicals
2-(Methylsulfinyl)benzeneboronic acid, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-(Methylsulfinyl)benzeneboronic acid, 97%, Thermo Scientific Chemicals

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Quantity:
250 mg
1 g
Catalog number H53209.MD
also known as H53209-MD
Price (USD)/ Each
124.00
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Quantity:
250 mg
Request bulk or custom format
Price (USD)/ Each
124.00
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2-(Methylsulfinyl)benzeneboronic acid, 97%, Thermo Scientific Chemicals
Catalog numberH53209.MD
Price (USD)/ Each
124.00
-
Add to cart
Specifications
Chemical Name or Material2-(Methylsulfinyl)benzeneboronic acid
CAS850567-97-4
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
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It is a useful intermediate in pharmaceutical intermediate. Boronic Acids are important chemical building blocks employed in cross coupling reactions. The ability of boronic acids to reversibly bind diol functional groups has been utilized for fluorescent detection of saccharides. The compound Bortezomib utilizes the boronic acid for its proteasome inhibitory effect.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is a useful intermediate in pharmaceutical intermediate. Boronic Acids are important chemical building blocks employed in cross coupling reactions. The ability of boronic acids to reversibly bind diol functional groups has been utilized for fluorescent detection of saccharides. The compound Bortezomib utilizes the boronic acid for its proteasome inhibitory effect.

Solubility
Slightly soluble in water.

Notes
Store in cool dry place. Ensure proper ventilation. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Virgil Percec.; Jin-Young Bae.; Dale H. Hill. Aryl Mesylates in Metal Catalyzed Homocoupling and Cross-Coupling Reactions. 2. Suzuki-Type Nickel-Catalyzed Cross-Coupling of Aryl Arenesulfonates and Aryl Mesylates with Arylboronic Acids.J. Org. Chem. 1995, 60 (4),1060-1065 .
  2. Manfred Baumgarth.; Norbert Beier.; Rolf Gericke. (2-Methyl-5-(methylsulfonyl)benzoyl)guanidine Na+/H+ Antiporter Inhibitors.J. Med. Chem. 1997, 40 (13),2017-2034 .