S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

Base Information

Chemical Name:S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate
CAS No.:1268161-62-1
Molecular Formula:C₂₁H₁₈N₄O₂S
Molecular Weight:390.466
Hs Code.:

Synonyms:S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

Suppliers and Price of S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

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 S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

There total 5 articles about S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate 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: 82.0%

: 865423-59-2
S-(5-(4-methoxybenzyl)-1,3,4-oxadiazole-2-yl) naphthalene-1-carbothioate

: 1268161-62-1
S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

Guidance literature:: With hydrazine hydrate; In ethanol; Reflux;
DOI:10.3390/molecules16021297

Reference yield:

: 104-01-8
4-Methoxyphenylacetic acid

: 1268161-62-1
S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

Guidance literature:: Multi-step reaction with 5 steps

1: Acidic conditions

2: hydrazine hydrate

3: potassium hydroxide

4: potassium hydroxide

5: hydrazine hydrate / ethanol / Reflux

With hydrazine hydrate; potassium hydroxide; In ethanol;
DOI:10.3390/molecules16021297

Reference yield:

: 23786-14-3
4-methoxy-phenyl acetic acid methyl ester

: 1268161-62-1
S-(5-(4-methoxybenzyl)-4-amino-1,2,4-triazole-3-yl) naphthalene-1-carbothioate

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate

2: potassium hydroxide

3: potassium hydroxide

4: hydrazine hydrate / ethanol / Reflux

With hydrazine hydrate; potassium hydroxide; In ethanol;
DOI:10.3390/molecules16021297