25485-88-5

Basic information

• Product Name: Benzoicacid,2-hydroxy-,cyclohexylester
• Synonyms: Benzoicacid,2-hydroxy-,cyclohexylester;Cyclohexyl salicylat;2-Hydroxybenzoic acid cyclohexyl;2-Hydroxybenzoic acid=cyclohexyl;cyclohexyl 2-hydroxybenzoate
• CAS NO: 25485-88-5
• Molecular Formula: C₁₃H₁₆O₃
• Molecular Weight: 220.26434
• Mol File: 25485-88-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 192-193 °C(Press: 30 Torr)
• Appearance: /
• Density: 1.17±0.1 g/cm3(Predicted)
• Vapor Pressure: 0.001-0.055Pa at 20℃
• PKA: 8.13±0.30(Predicted)
• CAS DataBase Reference: Benzoicacid,2-hydroxy-,cyclohexylester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoicacid,2-hydroxy-,cyclohexylester(25485-88-5)
• EPA Substance Registry System: Benzoicacid,2-hydroxy-,cyclohexylester(25485-88-5)

Safety Data

• Hazardous Substances Data: 25485-88-5(Hazardous Substances Data)

Usage

Chemical Properties

Cyclohexyl Salicylate is not found in nature. It is a colorless liquid, bp4 Pa 115°C, d2525 1.112, n20D 1.532–1.536, with aromatic, floral balsamic odor. It is used in perfumery instead of benzyl salicylate.

Upstream product

• 69-72-7 salicylic acid 
• 108-93-0 cyclohexanol 
• 119-36-8 methyl salicylate 

Downstream Products

• 69-72-7 salicylic acid 

Relevant articles and documents

POLYMERIZABLE MONOMERS AND METHOD OF POLYMERIZING THE SAME

Provided herein are photopolymerizable monomers, optionally for use as reactive diluents in a high temperature lithography-based photopolymerization process, a method of producing polymers using said photopolymerizable monomers, the polymers thus produced, and orthodontic appliances comprising the polymers.

LILIAN SURROGATE

Due to toxicological concerns, it may be desirable to replace the fragrance compound lilial with less problematic compounds without losing the creative power and quality regarding perfumes. The present invention addresses this need by using selected oxazolidines described herein.

Process for producing salicylic esters

There is provided a noble process for producing a salicylic ester for perfumes which comprises the step of transesterifying a salicylic lower alkyl ester with an alcohol having at least one carbon atom which is located adjacent to a hydroxyl-bonded carbon atom and has one or more hydrogen atoms bonded thereto, in the presence of a tin-based catalyst. The process of the present invention enables the salicylic ester to be produced at a high yield and is free from handling problems such as precipitation of solids in a distillation residue obtained after the reaction, and the catalyst used therein is reusable.