208655-73-6

Basic information

• Product Name: (1-(triisopropylsilyl)-1H-indol-3-yl)boronic acid
• Synonyms: (1-(triisopropylsilyl)-1H-indol-3-yl)boronic acid
• CAS NO: 208655-73-6
• Molecular Weight: 317.311
• Mol File: 208655-73-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (1-(triisopropylsilyl)-1H-indol-3-yl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(triisopropylsilyl)-1H-indol-3-yl)boronic acid(208655-73-6)
• EPA Substance Registry System: (1-(triisopropylsilyl)-1H-indol-3-yl)boronic acid(208655-73-6)

Safety Data

• Hazardous Substances Data: 208655-73-6(Hazardous Substances Data)

Usage

General Description

(1-(triisopropylsilyl)-1H-indol-3-yl)boronic acid is a boronic acid derivative that contains a triisopropylsilyl group attached to an indole ring. It is commonly used in organic chemistry as a reagent for the Suzuki-Miyaura coupling reaction, which is a widely used method for forming carbon-carbon bonds. (1-(triisopropylsilyl)-1H-indol-3-yl)boronic acid is an important building block in the synthesis of various biologically active molecules, including pharmaceuticals and natural products. Its boronic acid functionality allows it to participate in cross-coupling reactions with aryl halides or triflates, making it a valuable tool in the synthesis of complex organic molecules.

Upstream product

• 5419-55-6 Triisopropyl borate 
• 7732-18-5 water 
• 148249-36-9 3-bromo-1-(1,1,1-triisopropylsilyl)-1H-indole 
• 120-72-9 indole 
• 123191-00-4 1-(triisopropylsilyl)-1H-indole 
• 13154-24-0 triisopropylsilyl chloride 

Downstream Products

• 1365647-62-6 C₂₃H₃₀N₂O₂Si 
• 1365647-67-1 C₄₇H₃₀N₆ 
• 58421-67-3 1-methyl-3-(2-nitrophenyl)-1H-indole 
• 56366-31-5 3-(2-nitrophenyl)-1H-indole 
• 1365647-64-8 C₃₂H₂₁N₃O₂ 
• 1373266-35-3 C₅₈H₃₈N₄ 
• 1373266-34-2 C₂₆H₁₈N₂ 
• 1373266-33-1 C₂₆H₁₈N₂O₂ 
• 135531-86-1 camalexin 

Relevant articles and documents

NOVEL PYRIDIN-2(1H)ONE DERIVATIVES, THEIR PREPARATION AND THEIR USE FOR THE TREATMENT OF PAIN

The present invention concerns novel pyridin-2(1H)one derivatives, their process of preparation and their use in therapeutics, in particular as agents for treating and/or preventing pain.

NITROGENATED AROMATIC COMPOUND, ORGANIC SEMICONDUCTOR MATERIAL, AND ORGANIC ELECTRONIC DEVICE

Provided are a nitrogen-containing aromatic heterocyclic compound useful as an organic semiconductor material and an organic electronic device using this compound. The nitrogen-containing aromatic heterocyclic compound has a fused indole skeleton represented by the following formula (1), the organic semiconductor material contains the said compound, and the organic electronic device uses the said organic semiconductor material. In general formula (1), X is N-A', O, S, or Se; A is an alkyl group, a cycloalkyl group, an alkenyl group, an alkynyl group, an aromatic hydrocarbon group, or an aromatic heterocyclic group exclusive of a fused heterocycle consisting of 4 rings or more; and R is a hydrogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkynyl group, an aromatic hydrocarbon group, or an aromatic heterocyclic group exclusive of a fused heterocycle consisting of 4 rings or more.

Synthesis of (3-indolyl)heteroaromatics by Suzuki-Miyaura coupling and their inhibitory activity in lipid peroxidation

A variety of (3-indolyl)heteroaromatic compounds were synthesized by Suzuki-Miyaura coupling of 3-indolylboronic acid and halogenated heteroaromatics. 2-(3-Indolyl)thiophene showed potent inhibitory activity against lipid peroxidation by rat liver microsome.