Category: 80-46-6

Let’s face it, organic chemistry can seem difficult to learn, Computed Properties of https://www.ambeed.com/products/80-46-6.html, Especially from a beginner’s point of view. Like 80-46-6, Name is 4-tert-Amylphenol, molecular formula is indole-building-block, belongs to indole-building-block compound. In a document, author is Han, Qingshuai, introducing its new discovery.

In the past decades, C-H oxidative olefination of indole at C-2, C-3, C-4 and C-7 positions was well addressed. We report here a rhodium-catalyzed NH-indole-directed ortho C-H bond olefination of 2-arylindoles. This cross-dehydrogenative-coupling proved to be broad in substrate scope, tolerating a variety of functional groups. The synthesis of 6H-isoindolo[2,1-]indoles via rhodium-catalyzed ortho C-H olefination and subsequent intramolecular aza-Michael reaction of 2-arylindoles was also demonstrated.

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Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In an article, author is Singh, Thokchom Prasanta, once mentioned the application of 80-46-6, Name: 4-tert-Amylphenol, Name is 4-tert-Amylphenol, molecular formula is C11H16O, molecular weight is 164.24, MDL number is MFCD00002369, category is indole-building-block. Now introduce a scientific discovery about this category.

Synthesis of pi-conjugated green fluorescent protein chromophores analogs derived from amino acids are established. Indole and p-nitrophenyl tethered derivatives as the main structure could improve the thermal stability and optical property of the materials. The chromophores show good solubility in MeOH and CH3CN. They also show good thermal stability for practical applications. These compounds showed steady green light emissions in the range of 524-578 nm in solution.

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Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 80-46-6, Name is 4-tert-Amylphenol, SMILES is OC1=CC=C(C(C)(C)CC)C=C1, belongs to indole-building-block compound. In a document, author is Yong, Wanxiong, introduce the new discover, Recommanded Product: 4-tert-Amylphenol.

Pd-Catalyzed One-Pot Two-Step Synthesis of 2-(1H-indol-3-yl)-2-phenylindolin-3-ones from 2-Alkynyl Arylazides and Indoles

An efficient palladium-catalyzed one-pot two-step reaction of 2-alkynyl arylazides and indoles has been developed. The reaction proceeded well under mild reaction conditions and provided the 2-(1H-indole-3-yl)-2-phenylindolin-3-ones in good to excellent yields.This transformation involves a rearrangement of 1H-indole-3-sulfonates generated in situ and Mannich-type addition of indoline-3-ones.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 80-46-6 is helpful to your research. Recommanded Product: 4-tert-Amylphenol.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles