164461-18-1 | 1-Pyreneboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$9.00	$7.00
5g	98%	in stock	$17.00	$12.00
10g	98%	in stock	$29.00	$20.00
25g	98%	in stock	$49.00	$35.00
100g	98%	in stock	$195.00	$137.00

Description

• Catalog Number: AA86502
• Chemical Name: 1-Pyreneboronic acid
• CAS Number: 164461-18-1
• Molecular Formula: C16H11BO2
• Molecular Weight: 246.0683
• MDL Number: MFCD04974062
• SMILES: OB(c1ccc2c3c1ccc1c3c(cc2)ccc1)O

Computed Properties

• Complexity: 346
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

1-Pyreneboronic Acid is a versatile chemical compound that finds extensive application in chemical synthesis, particularly in the field of organic chemistry. This compound is highly valued for its ability to act as a key building block in the creation of various complex molecules due to its unique structural properties. In particular, 1-Pyreneboronic Acid is utilized as a critical component in the synthesis of organic materials, pharmaceuticals, and advanced materials.One of the primary applications of 1-Pyreneboronic Acid in chemical synthesis is its role as a powerful boronic acid derivative. As a boronic acid compound, it exhibits strong interactions with other molecules, particularly with compounds containing electron-rich functional groups such as alcohols and amines. This property enables 1-Pyreneboronic Acid to participate in diverse reactions, including Suzuki-Miyaura cross-coupling reactions, which are widely employed in the construction of carbon-carbon bonds.Furthermore, the presence of the pyrene moiety in 1-Pyreneboronic Acid confers additional reactivity and selectivity in chemical transformations. The aromatic nature of the pyrene ring imparts stability and conjugation to the molecule, leading to enhanced interactions with target substrates in synthetic processes. This feature makes 1-Pyreneboronic Acid a valuable tool in the development of novel organic compounds with specific properties and functionalities.Overall, 1-Pyreneboronic Acid serves as a crucial reagent in organic synthesis, enabling chemists to access a wide range of structurally diverse molecules through diverse synthetic pathways. Its unique structural characteristics and reactivity make it an indispensable component in the toolkit of synthetic chemists seeking to design and fabricate complex organic molecules with precision and efficiency.

Literature

• Determination of glyoxylic acid in urine by liquid chromatography with fluorescence detection, using a novel derivatization procedure based on the Petasis reaction.

  Analytical and bioanalytical chemistry 20120701

• Metal Ion Enhanced Charge Transfer in a Terpyridine-bis-Pyrene System.

  Sensors (Basel, Switzerland) 20090101