879487-14-6 | N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropanesulfonamide

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$283.00	$198.00
250mg	95%	in stock	$511.00	$358.00
1g	95%	in stock	$1,058.00	$740.00
5g	95%	in stock	$3,884.00	$2,719.00

Description

• Catalog Number: AX29026
• Chemical Name: N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropanesulfonamide
• CAS Number: 879487-14-6
• Molecular Formula: C15H22BNO4S
• Molecular Weight: 323.2154799999999
• MDL Number: MFCD31579396
• SMILES: O=S(=O)(C1CC1)Nc1ccc(cc1)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 500
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4

Upstream Synthesis Route

Cyclopropanesulfonamide, N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- is a versatile compound widely used in chemical synthesis processes. This compound is valued for its ability to serve as a key building block in the construction of complex organic molecules. Its unique structure allows for efficient incorporation into various synthetic pathways, enabling chemists to access diverse molecular architectures.In chemical synthesis, Cyclopropanesulfonamide, N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- plays a crucial role as a valuable reagent for cross-coupling reactions. By utilizing the boron-containing moiety, this compound facilitates the formation of carbon-carbon bonds, a fundamental step in the creation of intricate molecular structures. Furthermore, the presence of the sulfonamide group enhances the reactivity and selectivity of the compound, enabling chemists to target specific functional groups within a molecule.Overall, the strategic incorporation of Cyclopropanesulfonamide, N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]- in chemical synthesis allows for the streamlined construction of complex molecules with precision and efficiency. Its utility in cross-coupling reactions highlights its significance as a valuable tool for synthetic chemists seeking to expand their synthetic capabilities and access novel molecular frameworks.