40138-16-7 | 2-Formylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$8.00	$6.00
10g	98%	in stock	$10.00	$7.00
25g	98%	in stock	$22.00	$16.00
100g	98%	in stock	$80.00	$56.00
500g	98%	in stock	$399.00	$280.00

Description

• Catalog Number: AB47749
• Chemical Name: 2-Formylphenylboronic acid
• CAS Number: 40138-16-7
• Molecular Formula: C7H7BO3
• Molecular Weight: 149.9397
• MDL Number: MFCD00151822
• SMILES: O=Cc1ccccc1B(O)O
• NSC Number: 157839

Computed Properties

• Complexity: 138
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

With its versatile applications in chemical synthesis, 2-Formylphenylboronic acid serves as a crucial building block for the creation of various organic compounds. Its ability to undergo reactions such as Suzuki coupling, palladium-catalyzed cross-coupling, and metal-catalyzed oxidative coupling makes it an indispensable reagent in the production of pharmaceuticals, agrochemicals, and materials science. By serving as a precursor to functionalized benzene derivatives, 2-Formylphenylboronic acid enables the introduction of aldehyde moieties into complex molecular structures, facilitating the development of novel compounds with tailored properties and diverse functionalities. Its importance in the synthesis of biologically active molecules and advanced materials highlights its significance in modern organic chemistry research and industrial applications.

Literature

• Schiff base formation and recognition of amino sugars, aminoglycosides and biological polyamines by 2-formyl phenylboronic acid in aqueous solution.

  Organic & biomolecular chemistry 20120914

• Simple and efficient methods for discrimination of chiral diacids and chiral alpha-methyl amines.

  Organic & biomolecular chemistry 20120821

• Three-component chiral derivatizing protocols for NMR spectroscopic enantiodiscrimination of hydroxy acids and primary amines.

  The Journal of organic chemistry 20120106

• Asymmetric Strecker synthesis of α-arylglycines.

  The Journal of organic chemistry 20110805

• Phenylboronic-acid-based carbohydrate binders as antiviral therapeutics: monophenylboronic acids.

  Antiviral chemistry & chemotherapy 20100811

• Simple chiral derivatization protocols for 1H NMR and 19F NMR spectroscopic analysis of the enantiopurity of chiral diols.

  The Journal of organic chemistry 20090102

• Synthesis, characterization, and antifungal activity of boron-containing thiosemicarbazones.

  Chemistry & biodiversity 20081101

• Total synthesis of aristolactams via a one-pot suzuki-miyaura coupling/aldol condensation cascade reaction.

  Organic letters 20080821

• Direct one-pot synthesis of phenanthrenes via Suzuki-Miyaura coupling/aldol condensation cascade reaction.

  The Journal of organic chemistry 20080118

• Simple protocols for NMR analysis of the enantiomeric purity of chiral primary amines.

  Nature protocols 20080101

• Simple protocols for NMR analysis of the enantiomeric purity of chiral diols.

  Nature protocols 20080101

• An iminoboronate construction set for subcomponent self-assembly.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

• Simple protocol for NMR analysis of the enantiomeric purity of diols.

  Organic letters 20060511

• The fluorescence sensor for saccharide based on internal conversion.

  Luminescence : the journal of biological and chemical luminescence 20050101