1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline

Base Information

Chemical Name:1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline
CAS No.:296795-12-5
Molecular Formula:C₂₀H₂₁N₃S
Molecular Weight:335.473
Hs Code.:

Synonyms:1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline

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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-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline

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Technology Process of 1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline

There total 3 articles about 1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline 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:

: 3-phenyl-1-(5,6,7,8-tetrahydronaphthalene-2-yl)prop-2-en-1-one

: 79-19-6
thiosemicarbazide

: 296795-12-5
1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline

Guidance literature:: With sodium hydroxide; In ethanol; for 8h; Reflux;
DOI:10.3906/kim-1512-12

Reference yield:

: 100-52-7
benzaldehyde

: 296795-12-5
1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide

2: sodium hydroxide / ethanol / 8 h / Reflux

With sodium hydroxide; In ethanol;
DOI:10.3906/kim-1512-12

Reference yield:

: 774-55-0
6-Acetyl-1,2,3,4-tetrahydronaphthalene

: 296795-12-5
1-thiocarbamoyl-3-(5',6',7',8'-tetrahydronaphthalen-2'-yl)-5-phenyl-2-pyrazoline

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide

2: sodium hydroxide / ethanol / 8 h / Reflux

With sodium hydroxide; In ethanol;
DOI:10.3906/kim-1512-12