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Home  > 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

AI08663

1112209-32-1 | 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $76.00 $53.00 -   +
1g 97% in stock $200.00 $140.00 -   +
5g 97% in stock $753.00 $527.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI08663
Chemical Name: 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
CAS Number: 1112209-32-1
Molecular Formula: C13H16BClO3
Molecular Weight: 266.5283
MDL Number: MFCD18731011
SMILES: O=Cc1cc(ccc1Cl)B1OC(C(O1)(C)C)(C)C

 

Upstream Synthesis Route
  • 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile chemical compound commonly employed in chemical synthesis procedures. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural properties.In chemical synthesis, 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is primarily utilized as a key intermediate in the preparation of structurally complex compounds through Suzuki-Miyaura cross-coupling reactions. This reaction enables the coupling of the boron-containing compound with other suitable organic halides or pseudohalides, leading to the formation of diverse biaryl and heteroaryl compounds.The presence of the chloro group and the boron-containing moiety in 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde imparts significant synthetic utility, allowing for efficient derivatization and functionalization of the molecule to achieve desired molecular structures. This versatility makes it a valuable tool for organic chemists engaged in the synthesis of pharmaceuticals, agrochemicals, materials science, and other areas of applied chemistry.
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