873846-89-0

Basic information

• Product Name: Benzoic acid, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-, methyl ester
• CAS NO: 873846-89-0
• Molecular Formula: C15H18BF3O4
• Molecular Weight: 330.112
• Mol File: 873846-89-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-, methyl ester(873846-89-0)
• EPA Substance Registry System: Benzoic acid, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-, methyl ester(873846-89-0)

Safety Data

• Hazardous Substances Data: 873846-89-0(Hazardous Substances Data)

Upstream product

• 1483-56-3 2-bromo-5-(trifluoromethyl)benzoic acid 
• 73183-34-3 bis(pinacol)diborane 
• 1026355-57-6 methyl 2-bromo-5-(trifluoromethyl)benzoate 
• 26107-79-9 methyl 2-chloro-5-trifluoromethyl-benzoate 
• 2557-13-3 3-trifluoromethylbenzoic acid methyl ester 

Downstream Products

• 2557-13-3 3-trifluoromethylbenzoic acid methyl ester 
• 873846-90-3 Ethyl 1-benzyl-5-(2-(methoxycarbonyl)-4-(trifluoromethyl)phenyl)-1,2,3,6-tetrahydropyridine-4-carboxylate 

Relevant articles and documents

NOVEL SUBSTITUTED BIARYL COMPOUNDS AS INDOLEAMINE 2,3-DIOXYGENASE (IDO) INHIBITORS

Disclosed herein is a compound of formula (I), or a pharmaceutically acceptable salt thereof: Also disclosed herein are uses of a compound disclosed herein in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising a compound disclosed herein. Further disclosed herein are uses of a composition in the potential treatment or prevention of an IDO-associated disease or disorder.

Selenium-catalyzed C(sp3)-H acyloxylation: Application in the expedient synthesis of isobenzofuranones

Oxidative Se-catalyzed C(sp3)-H bond acyloxylation has been used to construct a diverse array of isobenzofuranones from simple ortho-allyl benzoic acid derivatives. The synthetic procedure employs mild reaction conditions and gives high chemoselectivity enabled by an inexpensive organodiselane catalyst. The presented approach offers a new synthetic pathway toward the core structures of phthalide natural products.

Ortho-C-H borylation of benzoate esters with bis(pinacolato)diboron catalyzed by iridium-phosphine complexes

Iridium complexes generated from [Ir(OMe)(COD)]2 and tris[3,5-bis(trifluoromethyl)phenyl]phosphine efficiently catalyzed the ortho-C-H borylation of benzoate esters with bis(pinacolato)diboron in octane at 80 °C to produce the corresponding ary