2-((2-Methylphenoxy)acetyl)-N-phenylhydrazinecarbothioamide

Base Information

Chemical Name:2-((2-Methylphenoxy)acetyl)-N-phenylhydrazinecarbothioamide
CAS No.:28743-95-5
Molecular Formula:C₁₆H₁₇N₃O₂S
Molecular Weight:315.396
Hs Code.:
European Community (EC) Number:657-325-1

Synonyms:2-((2-METHYLPHENOXY)ACETYL)-N-PHENYLHYDRAZINECARBOTHIOAMIDE;28743-95-5;2-[(2-methylphenoxy)acetyl]-N-phenylhydrazinecarbothioamide;ZINC00065334;STL481478;AKOS001025807;Z33099119

Suppliers and Price of 2-((2-Methylphenoxy)acetyl)-N-phenylhydrazinecarbothioamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-((2-Methylphenoxy)acetyl)-N-phenylhydrazinecarbothioamide

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:315.10414797
Heavy Atom Count:22
Complexity:372

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=CC=C1OCC(=O)NNC(=S)NC2=CC=CC=C2

Technology Process of 2-((2-Methylphenoxy)acetyl)-N-phenylhydrazinecarbothioamide

There total 1 articles about 2-((2-Methylphenoxy)acetyl)-N-phenylhydrazinecarbothioamide 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:

: 36304-37-7
o-tolyloxyacetic acid hydrazide

: 103-72-0
phenyl isothiocyanate

: 28743-95-5
C₁₆H₁₇N₃O₂S

Guidance literature:: In ethanol; Heating;
DOI:10.1016/S0223-5234(01)01252-1

Reference yield:

: 28743-95-5
C₁₆H₁₇N₃O₂S

: 4-[(3-(2-methylphenoxymethyl)-4-phenyl-1,2,4-triazol-5-yl)thioacetamido]antipyrine

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / 3 h / Heating

2: 92 percent / K₂CO₃ / acetone / 4 h / Heating

With sodium hydroxide; potassium carbonate; In acetone;
DOI:10.1016/S0223-5234(01)01252-1