1035235-28-9 | N-BOC-isoindoline-4-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$20.00	$14.00
250mg	96%	in stock	$49.00	$35.00
10g	96%	in stock	$1,940.00	$1,358.00
25g	96%	in stock	$3,867.00	$2,707.00

Description

• Catalog Number: AE25149
• Chemical Name: N-BOC-isoindoline-4-boronic acid, pinacol ester
• CAS Number: 1035235-28-9
• Molecular Formula: C19H28BNO4
• Molecular Weight: 345.2409199999999
• MDL Number: MFCD16652360
• SMILES: O=C(N1Cc2c(C1)c(ccc2)B1OC(C(O1)(C)C)(C)C)OC(C)(C)C

Computed Properties

• Complexity: 512
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 25
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3

Upstream Synthesis Route

The tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-dihydro-2H-isoindole-2-carboxylate plays a crucial role in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a versatile building block for the construction of complex molecules due to its unique structural features and reactivity.In chemical synthesis, this compound is commonly used as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its strategic placement within a synthetic route allows for the introduction of specific functional groups, stereochemical control, and overall structural manipulation to achieve the desired target molecule.Furthermore, the tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-dihydro-2H-isoindole-2-carboxylate exhibits excellent stability under a wide range of reaction conditions, making it a valuable tool for chemists seeking efficient and reliable methods for complex molecule synthesis. Its compatibility with various coupling reactions and its ability to undergo selective transformations make it a highly sought-after reagent in the synthetic organic chemistry community.