(E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide

Base Information

Chemical Name:(E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide
CAS No.:70161-75-0
Molecular Formula:C₁₉H₁₇N₃O₂S
Molecular Weight:351.429
Hs Code.:

Synonyms:(E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide

Suppliers and Price of (E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide

There total 3 articles about (E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide 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: 69.0%

: 121-33-5,8014-42-4
vanillin

: 42135-78-4
4-(1-naphthyl)-3-thiosemicarbazide

: 70161-75-0
(E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide

Guidance literature:: With acetic acid; In ethanol; water; for 1h; Reflux;
DOI:10.1016/j.bmc.2018.10.030

Reference yield:

: 551-06-4
1-isothiocyanatonaphthalene

: 70161-75-0
(E)-2-(4-hydroxy-3-methoxybenzylidene)-N-(naphthalen-1-yl)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine / isopropyl alcohol / 3 h / 20 °C

2: acetic acid / ethanol; water / 1 h / Reflux

With acetic acid; hydrazine; In ethanol; water; isopropyl alcohol;
DOI:10.1016/j.bmc.2018.10.030