283147-95-5

Basic information

• Product Name: 3-(4-Hydroxyphenyl)benzaldehyde
• Synonyms: 3-(4-Hydroxyphenyl)benzaldehyde;4-(3-Formylphenyl)phenol;4'-Hydroxy-biphenyl-3-carboxaldehyde
• CAS NO: 283147-95-5
• Molecular Formula: C13H10O2
• Molecular Weight: 198.22
• Mol File: 283147-95-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(4-Hydroxyphenyl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-Hydroxyphenyl)benzaldehyde(283147-95-5)
• EPA Substance Registry System: 3-(4-Hydroxyphenyl)benzaldehyde(283147-95-5)

Safety Data

• Hazardous Substances Data: 283147-95-5(Hazardous Substances Data)

Usage

General Description

3-(4-Hydroxyphenyl)benzaldehyde is a chemical compound with the molecular formula C13H10O2. It is also known as p-hydroxybenzaldehyde and is a white crystalline solid with a mild floral odor. 3-(4-Hydroxyphenyl)benzaldehyde is commonly used as a flavoring agent in the food and beverage industry and as an intermediate in the synthesis of other organic compounds. It can also be used in the production of fragrances, pharmaceuticals, and dyes. Additionally, 3-(4-Hydroxyphenyl)benzaldehyde has potential antioxidant properties and is being studied for its potential use in the treatment of various health conditions.

Upstream product

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• 1257724-90-5 C₁₁H₁₂BNO₅ 
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Relevant articles and documents

Multicomponent synthesis and anti-proliferative screening of biaryl triazole-containing cyclophanes

We report a practical two-step approach involving a Ugi 4-CR/ azide-alkyne cycloaddition for the synthesis of biaryl-containing cyclophanes. The series represents an extension of our previously reported macrocycles as an effort to enhance the anti-proliferative activity of this scaffold. In this variant, we incorporate a biphenyl moiety in the framework, thus enhancing the macrocycle size, lipophilicity, and structural diversity. Macrocycles were tested against different cell lines, being more cytotoxic against prostate (PC-3 and DU-145) and breast (MCF-7) tumor cells. Gratifyingly, the most active compound showed a significative enhancement of PC-3 growth inhibition with respect to our previous series, reaffirming the potential anti-proliferative activity of this kind of cyclophanes.

BIFEPRUNOX DERIVATIVES

The present invention relates to bifeprunox derivatives of the formula (I) wherein R1 is one substituent selected from 3-OH, 4-OH, 3-OSO3H and 4-OSO3H; R2 is H; or an N-oxide or a pharmaceutically acceptable salt, a solvate or hydrate thereof, which are p

Ionic Liquid Acceleration of Solid-Phase Suzuki-Miyaura Cross-Coupling Reactions

(Equation Presented) Room-temperature ionic liquids promote various transition metal-catalyzed reactions in the solution phase. Here, for the first time, we show that these effects are translatable to solid-phase reactions. The Suzuki-Miyaura cross-coupli