cas 867333-43-5|| where to buy (5-Cyano-2-methylphenyl)boronic acid

Product Name:(5-Cyano-2-methylphenyl)boronic acid

IUPAC Name:(5-cyano-2-methylphenyl)boronic acid

: CAS：867333-43-5; Molecular Formula：C8H8BNO2; Purity：95%+

: Catalog Number：CM135563; Molecular Weight：160.97

Packing Unit	Available Stock	Price($)
CM135563-5g	in stock	ƩƅƏ
CM135563-10g	in stock	ȋƅǺ
CM135563-25g	in stock	ǆœş

Inquiry: sales@chemenu.com

For R&D use only.

Inquiry Form

Chemical Name

CAS Number

Quantity*

Required Specifications*
(Assay %, Material Grade etc.)

Contact Name*

Contact Email*

Additional Notes

Verification code*

refresh

Product Details

: CAS NO:867333-43-5; Molecular Formula:C8H8BNO2; Melting Point:-; Smiles Code:CC1=C(C=C(C=C1)C#N)B(O)O; Density:

: Catalog Number:CM135563; Molecular Weight:160.97; Boiling Point:; MDL No:MFCD17015778; Storage:

Category Infos

: Boronic Acids and Esters; Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).; Boronic Acid For Sale; Find trusted boronic acid for sale. Any requirements and problems can ask us at any time.

: Benzenes; Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Column Infos

: Boronic Acids and Esters

: Benzenes

Product Other Information

Product Overview	(5-Cyano-2-methylphenyl)boronic acid, also known as 5-CN-2-MPBA, is an organic compound used in organic synthesis and medicinal chemistry. It is a boronic acid that is an important building block for the synthesis of biologically active compounds, such as kinase inhibitors, antibiotics, and other drugs. The compound has been studied for its potential applications in drug discovery, and its use in medicinal chemistry has become increasingly popular.
Synthesis and Application	The synthesis of (5-Cyano-2-methylphenyl)boronic acid can be achieved through several methods, including a two-step synthesis from 5-cyano-2-methylphenol and trimethyl borate, a one-step synthesis from 5-cyano-2-methylphenol and boron trifluoride etherate, and a one-step synthesis from 5-cyano-2-methylphenol and boron trifluoride. The two-step synthesis is the most commonly used method and involves the reaction of 5-cyano-2-methylphenol with trimethyl borate in the presence of an acid catalyst. The reaction produces (5-Cyano-2-methylphenyl)boronic acid as the main product, with other byproducts being formed in minor amounts. (5-Cyano-2-methylphenyl)boronic acid has been studied for its potential applications in drug discovery. It has been used as a building block for the synthesis of kinase inhibitors, antibiotics, and other drugs. It has also been used as a ligand in catalytic asymmetric reactions, as a catalyst for the synthesis of heterocyclic compounds, and as a reagent for the preparation of boronic esters. In addition, (5-Cyano-2-methylphenyl)boronic acid has been used in the synthesis of peptide-based probes for the detection of protein-protein interactions.
Future Directions	Future research on (5-Cyano-2-methylphenyl)boronic acid could focus on its potential applications in drug discovery and its biochemical and physiological effects. In addition, further studies could be conducted to explore the compound’s mechanism of action and its potential advantages and limitations for laboratory experiments. Other possible research directions include the development of new synthetic methods for the synthesis of (5-Cyano-2-methylphenyl)boronic acid, and the investigation of its use as a ligand in catalytic asymmetric reactions.