CAS 1761-63-3

4-Hydroxy[1,1′-biphenyl]-3-carboxaldehyde

Description:

4-Hydroxy[1,1′-biphenyl]-3-carboxaldehyde, also known by its CAS number 1761-63-3, is an organic compound characterized by its biphenyl structure with a hydroxyl group and an aldehyde functional group. This compound features a hydroxyl (-OH) group at the para position relative to the carboxaldehyde (-CHO) group on one of the phenyl rings, which contributes to its reactivity and potential applications in organic synthesis. It is typically a solid at room temperature and may exhibit solubility in organic solvents, depending on the specific conditions. The presence of both hydroxyl and aldehyde groups allows for various chemical reactions, including oxidation and condensation, making it useful in the synthesis of more complex organic molecules. Additionally, this compound may have applications in the fields of pharmaceuticals, agrochemicals, and materials science due to its potential biological activity and ability to act as a building block in chemical synthesis. Safety data should be consulted for handling and storage, as with all chemical substances.

Formula: C₁₃H₁₀O₂

InChI: InChI=1S/C13H10O2/c14-9-12-8-11(6-7-13(12)15)10-4-2-1-3-5-10/h1-9,15H

InChI key: InChIKey=NAUBSKHQFFCEMQ-UHFFFAOYSA-N

SMILES: C(=O)C=1C=C(C=CC1O)C2=CC=CC=C2

Synonyms:

• 4-Hydroxy[1,1′-biphenyl]-3-carboxaldehyde
• 4-Hydroxy-3-biphenylcarboxaldehyde
• 3-Biphenylcarboxaldehyde, 4-hydroxy-
• [1,1′-Biphenyl]-3-carboxaldehyde, 4-hydroxy-
• 5-Phenylsalicylaldehyde

[1,1'-Biphenyl]-3-carboxaldehyde, 4-hydroxy-

CAS: 1761-63-3

Formula: C₁₃H₁₀O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 198.2173

Ref: IN-DA00HZOS

2-Hydroxy-5-phenylbenzaldehyde

CAS: 1761-63-3

2-Hydroxy-5-phenylbenzaldehyde is a fluorescent probe that is used in the detection of amines and thiosemicarbazides. 2-Hydroxy-5-phenylbenzaldehyde has been shown to have antibacterial activity against bacteria such as subtilis and Staphylococcus aureus. This compound also emits fluorescence when it reacts with an amine or thiosemicarbazide, which can be used to detect these compounds. 2-Hydroxy-5-phenylbenzaldehyde also reacts with triethyl orthoformate under acidic conditions, producing ethylene and formic acid, which can be used to produce a volatile gas that can be detected by gas chromatography (GC).

Formula: C₁₃H₁₀O₂

Purity: Min. 95%

Molecular weight: 198.22 g/mol

Ref: 3D-BAA76163