28488-49-5

Basic information

• Product Name: Benzoic acid, 2-hydroxy-5-octyl-
• CAS NO: 28488-49-5
• Molecular Formula: C15H22O3
• Molecular Weight: 250.338
• Mol File: 28488-49-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-hydroxy-5-octyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-hydroxy-5-octyl-(28488-49-5)
• EPA Substance Registry System: Benzoic acid, 2-hydroxy-5-octyl-(28488-49-5)

Safety Data

• Hazardous Substances Data: 28488-49-5(Hazardous Substances Data)

Upstream product

• 119-36-8 methyl salicylate 
• 111-64-8 n-octanoic acid chloride 
• 124-38-9 carbon dioxide 
• 1806-26-4 p-Octylphenol 
• 78417-96-6 2-Hydroxy-5-octanoyl-benzoic acid methyl ester 
• 95772-48-8 2-Acetoxy-5-octyl-benzoic acid 

Downstream Products

• 78417-65-9 N-(4-Bromo-phenyl)-2-hydroxy-5-octyl-benzamide 

Relevant articles and documents

Micellar Catalysis of Organic Reactions. 25. Orientational Effects in Hydroxy-Functionalized Micelles

The basic hydrolysis of a number of aspirin derivatives in the presence of the hydroxy-functionalized micelles cetyl(2-hydroxyethyl)dimethylammonium bromide (CHEDAB), cetyl(2-hydroxypropyl)dimethylammonium bromide (CHPDAB), and (2-hydroxycetyl)trimethylammonium bromide (2-OH CTAB) and in the presence of cetyltrimethylammonium bromide (CTAB) has been compared.It has been found that of the hydroxy-functionalized micelles CHEDAB best discriminates between substrates with reaction centers at the micelle-water interface and those with reaction centers that are more deeplyburied in the micellar interior.This discrimination is shown in differences in the ratios of the optimum rates of hydrolysis in the hydroxy-functionalized micelles and in CTAB.It is also shown in the ratios of the calculated rates of reaction in the micellar pseudophase for the hydroxy-functionalized micelles and for CTAB.Thus the orientation of substrates within micellar aggregates is important in determining the magnitude of micellar catalysis.

Potential salicylamide antiplaque agents: In vitro antibacterial activity against Actinomyces viscosus

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