1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene

Base Information

Chemical Name:1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene
CAS No.:121006-91-5
Molecular Formula:C₂₃H₁₃BrN₄S
Molecular Weight:457.353
Hs Code.:

Synonyms:1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene

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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 1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene

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Technology Process of 1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene

There total 4 articles about 1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene 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: 70.0%

: 121006-83-5
3-[(4-Biphenyl-4-yl-thiazol-2-yl)-hydrazono]-5-bromo-1,3-dihydro-indol-2-one; hydrobromide

: 121006-91-5
1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene

Guidance literature:: With trichlorophosphate; at 120 - 130 ℃; for 4h;

Reference yield:

: 4553-11-1
2-(5-bromo-2,3-dihydro-2-oxo-1H-indol-3-ylidene)hydrazinecarbothioamide

: 121006-91-5
1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / ethanol; dimethylformamide / 2 h / Heating

2: 70 percent / POCl₃ / 4 h / 120 - 130 °C

With trichlorophosphate; In ethanol; N,N-dimethyl-formamide;

Reference yield:

: 135-73-9
2-Bromo-4'-phenylacetophenone

: 121006-91-5
1-Biphenyl-4-yl-7-bromo-3-thia-4,5,10,10b-tetraaza-cyclopenta[a]fluorene

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / ethanol; dimethylformamide / 2 h / Heating

2: 70 percent / POCl₃ / 4 h / 120 - 130 °C

With trichlorophosphate; In ethanol; N,N-dimethyl-formamide;