2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 61676-62-8

Ref. 3D-FI33118

Product Information

• Name: 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1-methylethoxy)-, 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaboralane, 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolan, 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxoborolane, 2-Isopropoxy-4,4,5,6-tetramethyl-1,3,2-dioxaboralane, 2-Isopropoxy-4,4′,5,5′-tetramethyl[1-3]dioxaborolane, 3-(Isopropoxycarbonyl)phenylboronic acid, 4,4,5,5-Tetramethyl-2-(1-methylethoxy)-1,3,2-dioxaborolane, 4,4,5,5-Tetramethyl-2-(Propan-2-Yloxy)-1,3,2-Dioxaborolane, 4,4,5,5-Tetramethyl-2-[(propan-2-yl)oxy]-1,3,2-dioxaborolane, 4,4,5,5-Tetramethyl-2-isopropoxy-1,3,2-dioxaborolane, Boric acid, cyclic tetramethylethylene isopropyl ester, Isopropoxy 4,4,5,5-tetramethyl-1,3,2-dioxaborolane, Isopropyl Pinacol Borate, Isopropyl pinacolyl borate, Isopropylpinacolylborate, PinBop

Description

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a synthetic chemical that has been shown to have antiviral activity against influenza virus and inhibit the synthesis of proteins in cancer cells. It inhibits the influenza virus from replicating by binding to the viral RNA polymerase and preventing it from transcribing viral RNA into proteins. 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane also binds to the boronic ester group of enzymes that are involved in plant metabolism and can be used as an herbicide. This chemical is synthesized by reacting boric acid with trimethoxysilane in an acidified water solution. The reaction produces hydrochloric acid which reacts with trimethoxysilane to form silanols. The silanols react with boric acid to produce 2

• Brand: Biosynth

Chemical properties

• Molecular weight: 186.06 g/mol
• Formula: C₉H₁₉BO₃
• Purity: Min. 95%
• Color/Form: Colourless Liquid
• InChI: InChI=1S/C9H19BO3/c1-7(2)11-10-12-8(3,4)9(5,6)13-10/h7H,1-6H3
• InChI key: InChIKey=MRWWWZLJWNIEEJ-UHFFFAOYSA-N
• SMILES: CC(C)OB1OC(C)(C)C(C)(C)O1