CAS 27329-70-0

2-Formylfuran-5-boronic acid

Description:

2-Formylfuran-5-boronic acid is an organic compound characterized by the presence of both a furan ring and a boronic acid functional group. The furan ring contributes to its aromatic properties, while the aldehyde group (formyl) and the boronic acid group provide reactivity that is useful in various chemical reactions, particularly in organic synthesis and medicinal chemistry. This compound typically appears as a solid and is soluble in polar solvents such as water and alcohols. Its boronic acid functionality allows for the formation of covalent bonds with diols, making it valuable in the development of boron-based reagents and catalysts. Additionally, 2-formylfuran-5-boronic acid can participate in cross-coupling reactions, which are essential in the synthesis of complex organic molecules. The compound's unique structure and reactivity make it a subject of interest in research areas such as materials science and pharmaceuticals. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and air.

Formula: C₅H₅BO₄

InChI: InChI=1/C5H5BO4/c7-3-4-1-2-5(10-4)6(8)9/h1-3,8-9H

SMILES: c1cc(B(O)O)oc1C=O

Synonyms:

• 5-Formyl-2-Furanylboronic Acid
• Ffba
• 5-Formyl-2-Furanboronic Acid
• 5-Formyl-2-Furylboronic Acid
• (5-Formyl-2-Furanyl)Boronic Acid
• 5-Formyl-2-Furyl Boronic Acid
• (5-Formylfuran-2-Yl)Boronic Acid
• 5-Formylfuran-2-boronic acid
• 5-Formylfuran-2-boronicacid

5-Formyl-2-furanboronic Acid (contains varying amounts of Anhydride)

CAS: 27329-70-0

Formula: C₅H₅BO₄

Purity: 95.0 to 115.0 %

Color and Shape: White to Brown powder to crystal

Molecular weight: 139.90

Ref: 3B-F0611

5-Formylfuran-2-boronic acid, 95%

CAS: 27329-70-0

As a bifunctional reagent used in the synthesis of -extended heteroarylfuran systems. Reactant involved in Suzuki coupling for synthesis of stable dye-sensitized solar cells. Reactant involved in synthesis of biologically active molecules including, heteroarylation for the synthesis of HIF-1 inhibi

Formula: C₅H₅BO₄

Purity: 95%

Color and Shape: Powder, Pale brown to brown

Molecular weight: 139.90

Ref: 02-L17920

2-Formylfuran-5-boronic acid

CAS: 27329-70-0

Formula: C₅H₅BO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 139.9018

Ref: IN-DA003844

2-Formylfuran-5-boronic acid

CAS: 27329-70-0

Formula: C₅H₅BO₄

Molecular weight: 139.90

Ref: 7W-GK7377

5-Formylfuran-2-boronic acid

CAS: 27329-70-0

5-Formylfuran-2-boronic acid

Formula: C₅H₅BO₄

Purity: 98%

Color and Shape: off white solid

Molecular weight: 139.9018g/mol

Ref: 54-OR8338

2-Formylfuran-5-boronic acid

CAS: 27329-70-0

Formula: C₅H₅BO₄

Purity: 97%

Color and Shape: Solid, Chunks or Crystalline Powder

Molecular weight: 139.9

Ref: 10-F011036

5-Formylfuran-2-boronic acid

CAS: 27329-70-0

5-Formylfuran-2-boronic acid is a compound that has been shown to be used in the synthesis of Pd complexes. This compound was found to inhibit the soluble guanylate cyclase and sirtuin 2 enzyme. It also has been shown to have anti-cancer effects, as it may inhibit cancer cell proliferation. 5-Formylfuran-2-boronic acid has been shown to increase the transport properties of potassium dichromate, which may be due to its acidic nature. This red fluorescent compound is soluble in organic solvents and can be activated by light. The optimum concentration of 5-Formylfuran-2-boronic acid is 3 mM in an acidic solution at room temperature.

Formula: C₅H₅BO₄

Purity: Min. 95%

Color and Shape: Yellow Solid

Molecular weight: 139.9 g/mol

Ref: 3D-FF10219

(5-Formylfuran-2-yl)boronic Acid

Controlled Product

CAS: 27329-70-0

Applications (5-Formylfuran-2-yl)boronic Acid is a reagent used in Suzuki cross-couplings with deactivated aryl bromides and activated aryl chlorides.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Trinh, T. N., et al.: Org. Biomol. Chem., 12, 9562-9571 (2014);

Formula: C₅H₅BO₄

Color and Shape: Beige

Molecular weight: 139.9

Ref: TR-F700345