118803-40-0 | 2-Hydroxymethyl-5-nitrophenylboronic acid, dehydrated

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$60.00	$42.00
1g	95%	in stock	$138.00	$96.00
5g	95%	in stock	$425.00	$297.00
25g	95%	in stock	$1,816.00	$1,271.00

Description

• Catalog Number: AE08577
• Chemical Name: 2-Hydroxymethyl-5-nitrophenylboronic acid, dehydrated
• CAS Number: 118803-40-0
• Molecular Formula: C7H6BNO4
• Molecular Weight: 178.9378
• MDL Number: MFCD04115657
• SMILES: [O-][N+](=O)c1ccc2c(c1)B(O)OC2

Computed Properties

• Complexity: 219
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1

Upstream Synthesis Route

6-Nitrobenzo[c][1,2]oxaborol-1(3H)-ol is a versatile compound widely used in chemical synthesis as a key building block. Its unique structure containing a nitro group and boron atom makes it highly valuable in the creation of various organic compounds.In organic synthesis, 6-Nitrobenzo[c][1,2]oxaborol-1(3H)-ol can act as a boron source in Suzuki-Miyaura cross-coupling reactions, enabling the formation of C-C bonds between aryl or vinyl halides and boronic acids or esters. This reaction is essential in the construction of complex organic molecules and pharmaceuticals.Additionally, this compound can participate in palladium-catalyzed C-N or C-O bond formation reactions, facilitating the introduction of nitrogen or oxygen functionalities into organic molecules. These reactions are crucial in the design and development of new materials and bioactive compounds.Furthermore, 6-Nitrobenzo[c][1,2]oxaborol-1(3H)-ol can undergo reduction reactions to yield the corresponding boronic acid or alcohol derivatives, which can be further manipulated in subsequent steps of a synthesis pathway. Its ability to serve as a versatile starting material highlights its significance in the field of organic chemistry.