201802-67-7 | 4-(Diphenylamino)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$14.00	$10.00
1g	95%	in stock	$18.00	$12.00
5g	95%	in stock	$26.00	$18.00
10g	95%	in stock	$28.00	$19.00
25g	95%	in stock	$56.00	$39.00
100g	95%	in stock	$217.00	$152.00
500g	95%	in stock	$977.00	$684.00

Description

• Catalog Number: AB03270
• Chemical Name: 4-(Diphenylamino)phenylboronic acid
• CAS Number: 201802-67-7
• Molecular Formula: C18H16BNO2
• Molecular Weight: 289.1361
• MDL Number: MFCD06798117
• SMILES: OB(c1ccc(cc1)N(c1ccccc1)c1ccccc1)O

Computed Properties

• Complexity: 301
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4

Upstream Synthesis Route

4-(Diphenylamino)phenylboronic acid is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. As a boronic acid derivative, it serves as an important building block in organic chemistry, especially in the realm of cross-coupling reactions.One significant application of 4-(Diphenylamino)phenylboronic acid is its use in Suzuki-Miyaura cross-coupling reactions. In this process, the boronic acid functionality of the compound reacts with an organoboron species, typically an aryl or vinyl boronate ester, in the presence of a palladium catalyst. This reaction allows for the formation of carbon-carbon bonds, facilitating the synthesis of complex organic molecules.Furthermore, the diphenylamino group in the structure of the compound can impart unique electronic properties and stereochemical effects to the final products of the cross-coupling reactions. This can be particularly advantageous in the design and synthesis of functional materials, pharmaceuticals, and agrochemicals.In summary, the application of 4-(Diphenylamino)phenylboronic acid in chemical synthesis is instrumental in enabling the efficient construction of diverse organic compounds through cross-coupling reactions, showcasing its significance in the field of organic chemistry.

Literature

• Synthesis of perylene dyes with multiple triphenylamine substituents.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20120910

• [Synthesis and spectral properties of a novel fluorinated triphenylamine derivative].

  Guang pu xue yu guang pu fen xi = Guang pu 20110201