Hydrazinecarbothioamide, N-(phenylmethyl)-2-(phenylmethylene)-

Base Information

Chemical Name:Hydrazinecarbothioamide, N-(phenylmethyl)-2-(phenylmethylene)-
CAS No.:7701-07-7
Molecular Formula:C15H15N3S
Molecular Weight:269.37
Hs Code.:
DSSTox Substance ID:DTXSID60392397

Synonyms:DTXSID60392397;Hydrazinecarbothioamide, N-(phenylmethyl)-2-(phenylmethylene)-;7701-07-7

Suppliers and Price of Hydrazinecarbothioamide, N-(phenylmethyl)-2-(phenylmethylene)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Hydrazinecarbothioamide, N-(phenylmethyl)-2-(phenylmethylene)-

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:269.09866866
Heavy Atom Count:19
Complexity:292

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC(=S)NN=CC2=CC=CC=C2

Technology Process of Hydrazinecarbothioamide, N-(phenylmethyl)-2-(phenylmethylene)-

There total 7 articles about Hydrazinecarbothioamide, N-(phenylmethyl)-2-(phenylmethylene)- 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:

: potassium; benzylthiocarbamoylsulfanyl-acetate

: 7701-07-7
benzaldehyde 4-benzyl-thiosemicarbazone

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / methanol / 0.75 h / Heating

2: methanol / 3 h / Heating

With hydrazine hydrate; In methanol;
DOI:10.1016/j.bmc.2006.05.047

Reference yield:

: 100-46-9
benzylamine

: 7701-07-7
benzaldehyde 4-benzyl-thiosemicarbazone

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / methanol; H₂O / cooling

1.2: methanol / 1 h / 40 °C

2.1: hydrazine hydrate / methanol / 0.75 h / Heating

3.1: methanol / 3 h / Heating

With potassium hydroxide; hydrazine hydrate; In methanol; water;
DOI:10.1016/j.bmc.2006.05.047