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

Nom du produit: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

Unité d'emballage	Stock disponible	Prix($)
CM334212-250mg	in stock	ŴƦ
CM334212-1g	in stock	ƦǧǊ

Pour une utilisation en R&D uniquement..

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: N° CAS:945556-95-6; Formule moléculaire:C17H25BN2O2; Point de fusion:-; Code SMILES:NC1=CC2=C(C=C1)C(B3OC(C)(C)C(C)(C)O3)=CN2C(C)C; Densité:

: Numéro de catalogue:CM334212; Poids moléculaire:300.21; Point d'ébullition:; N° Mdl:; Stockage:

: 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.