102170-51-4 | 3-Aminocarbonyl-5-nitrophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$65.00	$45.00
1g	98%	in stock	$177.00	$124.00
5g	98%	in stock	$572.00	$400.00
10g	98%	in stock	$945.00	$661.00
25g	98%	in stock	$1,878.00	$1,315.00

Description

• Catalog Number: AA08592
• Chemical Name: 3-Aminocarbonyl-5-nitrophenylboronic acid
• CAS Number: 102170-51-4
• Molecular Formula: C7H7BN2O5
• Molecular Weight: 209.9519
• MDL Number: MFCD07783870
• SMILES: OB(c1cc(cc(c1)C(=O)N)[N+](=O)[O-])O

Computed Properties

• Complexity: 267
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

(3-Carbamoyl-5-nitrophenyl)boronic acid is a versatile chemical reagent commonly utilized in chemical synthesis for its unique properties. This compound is a boronic acid derivative that contains a carbamoyl functional group and a nitro group attached to a phenyl ring. In organic synthesis, this reagent is primarily employed as a key building block in the construction of various complex molecular structures.One of the primary applications of (3-Carbamoyl-5-nitrophenyl)boronic acid is in the field of medicinal chemistry, where it is used in the synthesis of pharmaceutical intermediates and bioactive compounds. Due to its boronic acid moiety, this compound can participate in Suzuki-Miyaura cross-coupling reactions with aryl halides or triflates, leading to the formation of biaryl compounds. These biaryl derivatives are commonly found in a wide range of pharmaceuticals, agrochemicals, and materials science.Additionally, (3-Carbamoyl-5-nitrophenyl)boronic acid can also serve as a valuable component in the preparation of functionalized materials, such as polymers, liquid crystals, and electronic materials. Its ability to undergo various chemical transformations, including reduction, oxidation, and nucleophilic substitution reactions, makes it a versatile reagent for introducing specific functional groups into organic molecules.Overall, the application of (3-Carbamoyl-5-nitrophenyl)boronic acid in chemical synthesis offers researchers a powerful tool for accessing structurally diverse compounds with potential biological, material, and pharmaceutical relevance.