3-phenethyl-carbazole

Base Information

Chemical Name:3-phenethyl-carbazole
CAS No.:700863-09-8
Molecular Formula:C₂₀H₁₇N
Molecular Weight:271.362
Hs Code.:

Synonyms:

Suppliers and Price of 3-phenethyl-carbazole

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-phenethyl-carbazole

Chemical Property:

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Technology Process of 3-phenethyl-carbazole

There total 3 articles about 3-phenethyl-carbazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 412023-11-1
1-carbazol-3-yl-2-phenyl-ethanone

: 700863-09-8
3-phenethyl-carbazole

Guidance literature:: With potassium hydroxide; hydrazine hydrate; diethylene glycol;
DOI:10.1039/jr9540001341

Reference yield:

: 115552-48-2
N-carbazolyl-2-phenylacetamide

: 700863-09-8
3-phenethyl-carbazole

Guidance literature:: Multi-step reaction with 2 steps

1: aluminium chloride; nitrobenzene / 120 °C

2: hydrazine hydrate; potassium hydroxide; diethylene glycol

With potassium hydroxide; aluminium trichloride; hydrazine hydrate; nitrobenzene; diethylene glycol;
DOI:10.1039/jr9540001341

Reference yield:

: 86-74-8,105184-46-1,97960-57-1
9H-carbazole

: 700863-09-8
3-phenethyl-carbazole

Guidance literature:: Multi-step reaction with 3 steps

1: methyl magnesium chloride; diethyl ether / anschliessenden Erwaermen mit Phenylacetylchlorid

2: aluminium chloride; nitrobenzene / 120 °C

3: hydrazine hydrate; potassium hydroxide; diethylene glycol

With potassium hydroxide; aluminium trichloride; diethyl ether; methylmagnesium chloride; hydrazine hydrate; nitrobenzene; diethylene glycol;
DOI:10.1039/jr9540001341