9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene

Base Information

Chemical Name:9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene
CAS No.:82881-01-4
Molecular Formula:C₃₄H₂₅N₃
Molecular Weight:475.593
Hs Code.:

Synonyms:9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene

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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 9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene

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Technology Process of 9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene

There total 1 articles about 9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene 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: 92.0%

: 2201-70-9
(2,3-diphenylcyclopropen-1-ylidene)propanedinitrile

: 70109-15-8
1-(1-pyrrolidinyl)acenaphthylene

: 82881-01-4
9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene

Guidance literature:: In benzene; Ambient temperature;
DOI:10.1246/cl.1982.847

Reference yield: 94.0%

: 82881-01-4
9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene

: 82873-06-1
2-(7,9-diphenyl-8H-cyclopenta[a]acenaphthylen-8-ylidene)malononitrile

Guidance literature:: With hydrogenchloride; In acetic acid; Heating;
DOI:10.1246/cl.1982.847

Reference yield:

: 82881-01-4
9-dicyanomethylene-8,10-diphenyl-7-(1-pyrrolidinyl)-9H-cycloocta<1,2,3-ij>naphthalene

: 641-57-6
acecyclone

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / hydrochloric acid / acetic acid / Heating

2: 95 percent / KOH

With hydrogenchloride; potassium hydroxide; In acetic acid;
DOI:10.1246/cl.1982.847