cas 945556-95-6|| where to buy 1-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-6-amine

Product Name:1-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-6-amine

IUPAC Name:1-(propan-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-6-amine

Packing Unit	Available Stock	Price($)
CM334212-250mg	in stock	řƩ
CM334212-1g	in stock	ƩǎĜ

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: CAS NO:945556-95-6; Molecular Formula:C17H25BN2O2; Melting Point:-; Smiles Code:NC1=CC2=C(C=C1)C(B3OC(C)(C)C(C)(C)O3)=CN2C(C)C; Density:

: Catalog Number:CM334212; Molecular Weight:300.21; Boiling Point:; MDL No:; Storage:

: Indoles; Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.; indole company; As a indole company,we sincerely welcome the new and old friends from home and abroad to synergize with our company and share the benefits and opportunities.

Product Overview	1-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-6-amine (945556-95-6) is a synthetic compound that has recently been studied for its potential applications in a variety of scientific research fields. 1-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-6-amine is a derivative of the indole family of compounds, and is known to have a wide range of pharmacological activities, including anti-inflammatory, anti-oxidant, and anti-cancer effects.
Chemical Properties	1-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-6-amine is a reactive compound, often utilized as a starting material or intermediate in various chemical reactions and synthesis processes.
Synthesis and Application	1-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-6-amine has been studied for its potential applications in a variety of scientific research fields. For example, it has been used as a tool to study the effects of indole derivatives on the modulation of protein-protein interactions, as well as to investigate the binding of indole derivatives to DNA and RNA. Additionally, it has been used to study the effects of indole derivatives on the inhibition of enzymes involved in cancer cell proliferation, as well as to investigate the effects of indole derivatives on the regulation of gene expression.