19820-51-0

Basic information

• Product Name: Benzaldehyde, 2-(benzoyloxy)-
• CAS NO: 19820-51-0
• Molecular Formula: C14H10O3
• Molecular Weight: 226.232
• Mol File: 19820-51-0.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(benzoyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(benzoyloxy)-(19820-51-0)
• EPA Substance Registry System: Benzaldehyde, 2-(benzoyloxy)-(19820-51-0)

Safety Data

• Hazardous Substances Data: 19820-51-0(Hazardous Substances Data)

Upstream product

• 90-02-8 salicylaldehyde 
• 98-88-4 benzoyl chloride 
• 89290-01-7 salicylaldehyde, thallium(I) salt 
• 100-42-5 styrene 
• 93-58-3 benzoic acid methyl ester 
• 70-11-1 α-bromoacetophenone 
• 100-51-6 benzyl alcohol 
• 100-52-7 benzaldehyde 
• 40138-16-7 2-formylbenzene boronic acid 
• 65-85-0 benzoic acid 
• 108-88-3 toluene 
• 92103-18-9 Benzoic acid 2-chloromethyl-phenyl ester 
• 89-95-2 2-methyl-benzyl alcohol 
• 3116-83-4 sodium salicylate 

Downstream Products

• 30923-59-2 2-hydroxybenzyl benzoate 
• 146952-31-0 2-benzoyloxy-benzyl alcohol 
• 1485-70-7 N-benzylbenzamide 
• 479354-25-1 C₂₀H₁₄BrNO₂ 
• 479354-15-9 C₂₀H₁₅NO₂ 
• 1301626-55-0 C₂₈H₂₄N₂O₄ 
• 1301626-53-8 C₂₇H₂₂N₂O₄ 

Relevant articles and documents

2-formyl-3,6-bis(hydroxymethyl)phenyl benzoate in Electrochemical Dry Cell

Solvated organic compound with the general formula 2-formyl-3,6-bis(hydroxymethyl)phenyl benzoate [C16H14O5] was synthesized. Fourier-transform infrared (FTIR), Mass Spectrometry (MS) and X-ray powder analytical methods were used here for structure elucidation. Characterization revealed a triclinic geometry with space group P1. The refined unit cell parameters are, a = 15.196 ?, b = 14.882 ? and c = 14.606 ?. Development in present work is an idea of the organic electrochemical dry cell. Electrochemists with an idea in vitro/vivo development in present assay are openly encouraged for supporting exploration.

Copper-catalyzed chemoselective oxidative o-aroylation of 2-acetylphenols, alkyl salicylates and 1,3-dicarbonyl compounds using styrene derivatives

A novel copper-catalyzed chemoselective oxidative O-aroylation of 2-acetylphenols, alkyl salicylates and 1,3-dicarbonyl compounds with a wide range of styrene derivatives are described. This approach provides an efficient chemoselective preparation of phenol, alkyl salicylate and enol esters in good to excellent yields. This method represents an alternative protocol for the classical esterification reactions.

Solid-Phase Benzoylation of Phenols and Alcohols in Microwave Reactor: An Ecofriendly Protocol

An efficient solid-phase benzoylation of phenols and alcohols was developed under microwave irradiation. A stoichiometric amount of benzoyl chloride was sufficient to carry out the reaction. This benzoylation features short reaction time, good yields, and easy workup procedures. Furthermore, the scope of the reaction was extended to prepare 3,5-dinitrobenzoyl derivatives of alcohols.