1431794-52-3

Basic information

• Product Name: potassium trifluoro(4-methylphenethyl)borate
• Synonyms: potassium trifluoro(4-methylphenethyl)borate
• CAS NO: 1431794-52-3
• Molecular Weight: 226.091
• Mol File: 1431794-52-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: potassium trifluoro(4-methylphenethyl)borate(CAS DataBase Reference)
• NIST Chemistry Reference: potassium trifluoro(4-methylphenethyl)borate(1431794-52-3)
• EPA Substance Registry System: potassium trifluoro(4-methylphenethyl)borate(1431794-52-3)

Safety Data

• Hazardous Substances Data: 1431794-52-3(Hazardous Substances Data)

Upstream product

• 622-97-9 1-ethenyl-4-methylbenzene 

Downstream Products

• 32327-69-8 1-cyano-2-(4'-methylphenyl)ethane 
• 342819-73-2 4-methyl-N-[2-(4-methylphenyl)ethyl]benzenesulfonamide 
• 699-02-5 4-Methylphenethyl alcohol 

Relevant articles and documents

Visible-Light-Mediated Aerobic Oxidation of Organoboron Compounds Using in Situ Generated Hydrogen Peroxide

A simple and general visible-light-mediated oxidation of organoboron compounds has been developed with rose bengal as the photocatalyst, substoichiometric Et3N as the electron donor, as well as air as the oxidant. This mild and metal-free protocol shows a broad substrate scope and provides a wide range of aliphatic alcohols and phenols in moderate to excellent yields. Notably, the robustness of this method is demonstrated on the stereospecific aerobic oxidation of organoboron compounds.

Conformational restriction approach to BACE1 inhibitors II: SAR study of the isocytosine derivatives fixed with a cis-cyclopropane ring

To improve the efficacy of the conformationally restricted BACE1 inhibitors, structural modifications were investigated using two strategies: (a) modification of the terminal aromatic ring and (b) insertion of a spacer between the aromatic rings. In the latter approach, another type of inhibitor 17 bearing an ethylene spacer between two aromatic rings was found to exhibit good BACE1 inhibitory activity, while the corresponding conformationally unrestricted compound 25 showed no activity. This result revealed an interesting effect of a conformational restriction with a cyclopropane ring.