94200-04-1

Basic information

• Product Name: 2-phenylpropyl salicylate
• Synonyms: 2-phenylpropyl salicylate;Salicylic acid 2-phenylpropyl ester
• CAS NO: 94200-04-1
• Molecular Formula: C16H16O3
• Molecular Weight: 256.29644
• EINECS: 303-480-2
• Mol File: 94200-04-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 379.3°Cat760mmHg
• Flash Point: 155.7°C
• Appearance: /
• Density: 1.163g/cm³
• Vapor Pressure: 2.71E-06mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 2-phenylpropyl salicylate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenylpropyl salicylate(94200-04-1)
• EPA Substance Registry System: 2-phenylpropyl salicylate(94200-04-1)

Safety Data

• Hazardous Substances Data: 94200-04-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H16O3/c1-12(13-7-3-2-4-8-13)11-19-16(18)14-9-5-6-10-15(14)17/h2-10,12,17H,11H2,1H3

Upstream product

• 1393802-61-3 (R)-2-benzoyloxy-2-phenylpropionaldehyde 
• 34713-70-7 2-Phenylpropanal 
• 94-36-0 dibenzoyl peroxide 
• 1393802-62-4 (S)-2-benzoyloxy-2-phenylpropionaldehyde 

Relevant articles and documents

Organocatalytic asymmetric α-benzoyloxylation of α-branched aldehydes and enals: A useful approach to oxygenated quaternary stereocenters

Direct asymmetric α-benzoyloxylation of α-branched aldehydes and α-branched enals via enamine and dienamine catalysis was used to construct quaternary oxygenated stereocenters with good yields and moderate to good enantioselectivity. This method uses an inexpensive and readily available cinchona alkaloid-derived primary amine as the catalyst, benzoyl peroxide as the oxygen source, and stoichiometric amounts of the aldehyde substrates, providing simple metal-free access to valuable protected 2-hydroxyaldehyde derivatives.