C₁₈H₁₅N₃

Base Information

Chemical Name:C₁₈H₁₅N₃
CAS No.:228106-69-2
Molecular Formula:C₁₈H₁₅N₃
Molecular Weight:273.337
Hs Code.:

C<sub>18</sub>H<sub>15</sub>N<sub>3</sub>

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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 C₁₈H₁₅N₃

Chemical Property:

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Technology Process of C₁₈H₁₅N₃

There total 4 articles about C₁₈H₁₅N₃ 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:

: 1150-62-5
N-phenylcarbazole

: 228106-69-2
C₁₈H₁₅N₃

Guidance literature:: Multi-step reaction with 2 steps

1: acetic anhydride; copper(II) nitrate; acetic acid / 0.5 h

2: palladium on activated charcoal; hydrazine hydrate / ethanol / 6 h / Reflux

With palladium on activated charcoal; acetic anhydride; copper(II) nitrate; hydrazine hydrate; acetic acid; In ethanol;
DOI:10.1002/jccs.201100601

Reference yield:

: 54311-36-3
3,6-dinitro-9-phenyl-carbazole

: 228106-69-2
C₁₈H₁₅N₃

Guidance literature:: With palladium on activated charcoal; hydrazine hydrate; In ethanol; for 6h; Reflux;
DOI:10.1002/jccs.201100601

Reference yield:

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

: 228106-69-2
C₁₈H₁₅N₃

Guidance literature:: Multi-step reaction with 3 steps

1: 18-crown-6 ether; copper; potassium carbonate / 1,2-dichloro-benzene / 20 h / 190 °C

2: acetic anhydride; copper(II) nitrate; acetic acid / 0.5 h

3: palladium on activated charcoal; hydrazine hydrate / ethanol / 6 h / Reflux

With 18-crown-6 ether; palladium on activated charcoal; acetic anhydride; copper; potassium carbonate; copper(II) nitrate; hydrazine hydrate; acetic acid; In ethanol; 1,2-dichloro-benzene;
DOI:10.1002/jccs.201100601