1,3-benzodioxole-5-carbaldehyde N-(4-methylphenyl)thiosemicarbazone

Base Information

Chemical Name:1,3-benzodioxole-5-carbaldehyde N-(4-methylphenyl)thiosemicarbazone
CAS No.:97724-22-6
Molecular Formula:C₁₆H₁₅N₃O₂S
Molecular Weight:313.38
Hs Code.:
Mol file:97724-22-6.mol

Synonyms:(E)-2-(benzo[d][1,3]dioxol-5-ylmethylene)-N-(p-tolyl)hydrazinecarbothioamide

Suppliers and Price of 1,3-benzodioxole-5-carbaldehyde N-(4-methylphenyl)thiosemicarbazone

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

Aronis compounds
1,3-benzodioxole-5-carbaldehydeN-(4-methylphenyl)thiosemicarbazone
50mg
$ 50.00

Aronis compounds
1,3-benzodioxole-5-carbaldehydeN-(4-methylphenyl)thiosemicarbazone
10mg
$ 20.00

Total 0 raw suppliers

Chemical Property of 1,3-benzodioxole-5-carbaldehyde N-(4-methylphenyl)thiosemicarbazone

Chemical Property:

Purity/Quality:: 1,3-benzodioxole-5-carbaldehydeN-(4-methylphenyl)thiosemicarbazone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1,3-benzodioxole-5-carbaldehyde N-(4-methylphenyl)thiosemicarbazone

There total 4 articles about 1,3-benzodioxole-5-carbaldehyde N-(4-methylphenyl)thiosemicarbazone 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: 60.0%

: 120-57-0,30024-74-9
piperonal

: 13278-67-6
4-(4-methylphenyl)-3-thiosemicarbazide

: 97724-22-6
(E)-2-(benzo[d][1,3]dioxol-5-ylmethylene)-N-(p-tolyl)hydrazinecarbothioamide

Guidance literature:: With acetic acid; In ethanol; water; for 1h; Reflux;
DOI:10.21577/0103-5053.20170146

Reference yield:

: 622-59-3
1-isothiocyanato-4-methylbenzene

: 97724-22-6
(E)-2-(benzo[d][1,3]dioxol-5-ylmethylene)-N-(p-tolyl)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

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

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

With hydrazine hydrate; acetic acid; In ethanol; water; isopropyl alcohol;
DOI:10.21577/0103-5053.20170146