1001200-61-8

Basic information

• Product Name: 5-METHYL-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZO[B]THIOPHENE
• Synonyms: 5-METHYL-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZO[B]THIOPHENE;4,4,5,5-tetraMethyl-2-(5-Methylbenzo[b]thiophen-2-yl)-1,3,2-dioxaborolane;Benzo[b]thiophene, 5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxabo
• CAS NO: 1001200-61-8
• Molecular Formula: C15H19BO2S
• Molecular Weight: 274.18616
• Mol File: 1001200-61-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-METHYL-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZO[B]THIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHYL-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZO[B]THIOPHENE(1001200-61-8)
• EPA Substance Registry System: 5-METHYL-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZO[B]THIOPHENE(1001200-61-8)

Safety Data

• Hazardous Substances Data: 1001200-61-8(Hazardous Substances Data)

Upstream product

• 76-09-5 2,3-dimethyl-2,3-butane diol 

Relevant articles and documents

Optimizing cell permeation of an antibiotic resistance inhibitor for improved efficacy

Benzo[b]thiophene-2-ylboronic acid, 1, is a 27 nM inhibitor of the class C β-lactamase AmpC and potentiates the activity of β-lactam antibiotics in bacteria that express this and related enzymes. As is often true, the potency of compound 1 against the enz

gem-dibromomethylarenes: A convenient substitute for noncommercial aldehydes in the Knoevenagel-Doebner reaction for the synthesis of α,β-unsaturated carboxylic acids

(Chemical Equation Presented) A facile synthesis of α,β- unsaturated carboxylic acids from gem-dibromomethylarenes is described. gem-Dibromomethylarenes are employed for the first time in the Knoevenagel-Doebner reaction as aldehyde equivalents for the efficient synthesis of α,β-unsaturated carboxylic acids.