147578-43-6

Basic information

• Product Name: Benzoic acid, 2-(2-methylpropoxy)-
• Synonyms: 2-Isobutoxybenzoic acid
• CAS NO: 147578-43-6
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.2271
• Mol File: 147578-43-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 313.257 °C at 760 mmHg
• Flash Point: 119.087 °C
• Density: 1.104 g/cm3
• CAS DataBase Reference: Benzoic acid, 2-(2-methylpropoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-(2-methylpropoxy)-(147578-43-6)
• EPA Substance Registry System: Benzoic acid, 2-(2-methylpropoxy)-(147578-43-6)

Safety Data

• Hazardous Substances Data: 147578-43-6(Hazardous Substances Data)

Upstream product

• 119-36-8 methyl salicylate 
• 147578-45-8 2-chloro-6-isobutoxybenzoic acid 
• 21018-09-7 methyl 2-(isobutyloxy)benzoate 
• 78-83-1 2-methyl-propan-1-ol 
• 94-36-0 dibenzoyl peroxide 
• 54514-31-7 1-bromo-2-isobutoxybenzene 
• 124-38-9 carbon dioxide 

Downstream Products

• 268564-38-1 methyl 2-(2-isobutoxyphenyl)acetate 
• 503809-63-0 8-(2-isobutoxy-phenyl)-3-isobutyl-1-methyl-3,7-dihydro-purine-2,6-dione 

Relevant articles and documents

Thermodynamic properties of isomeric iso-butoxybenzoic acids: Experimental and theoretical study

Standard (p° = 0.1 MPa) molar enthalpies of formation at the temperature T = 298.15 K of the 2-, 3-, and 4-iso-butoxybenzoic acids were measured using the combustion calorimetry. Standard molar enthalpies of vaporization and sublimation were derived from

NOVEL COMPOUNDS AND MEDICINAL USE THEREOF

A compound comprising the atom corresponding to N3 and the two or more atoms selected from N1, N2, N4 and N5, said atoms constitute the pharmacophore represented by the following formula: wherein Nsu

Cyclic Nucleotide Phosphodiesterase Inhibition by Imidazopyridines: Analogues of Sulmazole and Isomazole as Inhibitors of the cGMP Specific Phosphodiesterase

The synthesis and phosphodiesterase (PDE) inhibitory profile of a series of imidazopyridines, including sulmazole and isomazole, on separated PDE isoenzymes are described.The results show that both sulmazole and isomazole are weak inhibitors of PDE III, and their inotropic activity is unlikely to be due to PDE III inhibition alone.Surprisingly, both compounds were found to be significant inhibitors of the cGMP specific isoenzyme, PDE V, and a series of simple 2-substituted phenylimidazopyridines have been made to investigate the SAR of PDE activity.This has been shown to be sensitive to chain length, polarity, and the nature of the heteroatom linking group.Potent PDE V inhibitors, many of which are also significant inhibitors of PDE IV, have been identified.