22890-52-4

Basic information

• Product Name: 3-(1-propyl)-2-hydroxybenzoic acid
• Synonyms: 3-(1-propyl)-2-hydroxybenzoic acid
• CAS NO: 22890-52-4
• Molecular Weight: 180.203
• Mol File: 22890-52-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-(1-propyl)-2-hydroxybenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-propyl)-2-hydroxybenzoic acid(22890-52-4)
• EPA Substance Registry System: 3-(1-propyl)-2-hydroxybenzoic acid(22890-52-4)

Safety Data

• Hazardous Substances Data: 22890-52-4(Hazardous Substances Data)

Upstream product

• 92810-83-8 2-hydroxy-3-propenyl-benzoic acid 
• 64-17-5 ethanol 
• 42729-96-4 2-Hydroxy-3-(2-propenyl)-benzoesaeure 
• 644-35-9 5-propylphenol 
• 124-38-9 carbon dioxide 

Downstream Products

• 644-35-9 5-propylphenol 
• 108294-79-7 (4-Chloro-phenyl)-(2-hydroxy-3-propyl-phenyl)-methanone 
• 108294-70-8 (2-Hydroxy-3-propyl-phenyl)-phenyl-methanone 

Relevant articles and documents

Improved Preparation of the Clathrate Host Compound Tri-o-thymotide and Related Trisalicylide Derivatives

In order to improve the relatively low yield (ca. 35percent) previously observed in the synthesis of tri-o-thymotide (TOT, 1) from o-thymotic acid (2), the cyclodehydration was studied using a variety of conditions.The low yield is due to the formation of di-o-thymotide (DOT, 3), previously reported, and at least three other products (4-6), which apparently result from the acid-catalyzed decarboxylation of 2 and subsequent condensation with thymol (7).Using pyridine as a solvent, side-product formation is inhibited.Under appropriate conditions, namely, neat POCl3 at 50 deg C, the yield of 1 is 93percent.Other salicylic acid derivatives also give high yields of the corresponding "trimers" under these conditions, thus providing a general, improved preparation of a family of potential clathrate host substances.