5-(4-Methylphenoxymethyl)-4H-1,2,4-triazole-3-thiol

Base Information

Chemical Name:5-(4-Methylphenoxymethyl)-4H-1,2,4-triazole-3-thiol
CAS No.:143540-96-9
Molecular Formula:C10H11N3OS
Molecular Weight:221.283
Hs Code.:
European Community (EC) Number:872-570-6
Nikkaji Number:J1.586.208D
Mol file:143540-96-9.mol

Synonyms:5-(4-Methylphenoxymethyl)-4H-1,2,4-triazole-3-thiol;143540-96-9;5-[(4-methylphenoxy)methyl]-1,2-dihydro-1,2,4-triazole-3-thione;5-p-Tolyloxymethyl-4H-[1,2,4]triazole-3-thiol;AKOS000117329;EN300-06409;AB00719220-01;5-[(4-methylphenoxy)methyl]-4H-1,2,4-triazole-3-thiol

Suppliers and Price of 5-(4-Methylphenoxymethyl)-4H-1,2,4-triazole-3-thiol

Supply Marketing:

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

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Chemical Property of 5-(4-Methylphenoxymethyl)-4H-1,2,4-triazole-3-thiol

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:221.06228316
Heavy Atom Count:15
Complexity:272

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)OCC2=NC(=S)NN2

Technology Process of 5-(4-Methylphenoxymethyl)-4H-1,2,4-triazole-3-thiol

There total 5 articles about 5-(4-Methylphenoxymethyl)-4H-1,2,4-triazole-3-thiol 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: 86.5%

: 121068-31-3
C₁₀H₁₃N₃O₂S

: 143540-96-9
2-(4-methylphenyl)oxymethyl-5-mercapto-1,2,4-triazole

Guidance literature:: With sodium hydroxide; at 95 ℃; for 4h;
DOI:10.1002/jhet.5570380418

Reference yield:

: 940-64-7
2-(4-methylphenoxy)acetic acid

: 143540-96-9
2-(4-methylphenyl)oxymethyl-5-mercapto-1,2,4-triazole

Guidance literature:: Multi-step reaction with 4 steps

1: p-toluenesulfonic acid / 5 h / Heating

2: hydrazine hydrate / ethanol / 3 h / Heating

3: aq. HCl / 4 h / Heating

4: 86.5 percent / 8 percent aq. NaOH / 4 h / 95 °C

With hydrogenchloride; sodium hydroxide; toluene-4-sulfonic acid; hydrazine hydrate; In ethanol;
DOI:10.1002/jhet.5570380418

Reference yield:

: 67028-40-4
ethyl (4-methylphenoxy)acetate

: 143540-96-9
2-(4-methylphenyl)oxymethyl-5-mercapto-1,2,4-triazole

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / ethanol / 3 h / Heating

2: aq. HCl / 4 h / Heating

3: 86.5 percent / 8 percent aq. NaOH / 4 h / 95 °C

With hydrogenchloride; sodium hydroxide; hydrazine hydrate; In ethanol;
DOI:10.1002/jhet.5570380418