1150271-44-5 | Oxindole-4-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$36.00	$26.00
250mg	95%	in stock	$60.00	$42.00
1g	95%	in stock	$161.00	$113.00
5g	95%	in stock	$576.00	$403.00
25g	95%	in stock	$2,625.00	$1,837.00

Description

• Catalog Number: AA20177
• Chemical Name: Oxindole-4-boronic acid, pinacol ester
• CAS Number: 1150271-44-5
• Molecular Formula: C14H18BNO3
• Molecular Weight: 259.1086
• MDL Number: MFCD11504971
• SMILES: O=C1Cc2c(N1)cccc2B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 380
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1

Upstream Synthesis Route

1,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indol-2-one is a versatile compound widely utilized in chemical synthesis processes. This molecule serves as a crucial building block in the development of various organic compounds due to its unique structure and reactivity. Specifically, in chemical synthesis, this compound is commonly employed as a key intermediate in the construction of complex organic molecules.One prominent application of 1,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indol-2-one is in the synthesis of pharmaceutical compounds. Its structural features make it an ideal precursor in the preparation of drug candidates and active pharmaceutical ingredients. By incorporating this compound into synthetic pathways, chemists can access novel chemical entities with potential therapeutic properties.Furthermore, 1,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indol-2-one plays a pivotal role in the development of agrochemicals, fine chemicals, and materials science. Its versatility and compatibility with a wide range of organic reactions make it a valuable asset in the synthesis of various specialty chemicals. Moreover, this compound enables chemists to streamline synthetic routes and enhance the overall efficiency of chemical processes.In conclusion, the strategic utilization of 1,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indol-2-one in chemical synthesis underscores its significance as a fundamental building block in organic chemistry. Its applications span across diverse sectors, highlighting its importance in facilitating the creation of innovative compounds with potential industrial and pharmaceutical applications.