N-Phenyl-2-(phthalazin-1-yl)hydrazinecarbothioamide

Base Information

Chemical Name:N-Phenyl-2-(phthalazin-1-yl)hydrazinecarbothioamide
CAS No.:61051-54-5
Molecular Formula:C15H13N5S
Molecular Weight:295.368
Hs Code.:
DSSTox Substance ID:DTXSID80423490
Wikidata:Q82235721
Pharos Ligand ID:CXR422BXTMYJ
ChEMBL ID:CHEMBL3924500

Synonyms:61051-54-5;CHEMBL3924500;N-Phenyl-2-(phthalazin-1-yl)hydrazinecarbothioamide;ST50432161;DTXSID80423490;BDBM50204745;AKOS003348640

Suppliers and Price of N-Phenyl-2-(phthalazin-1-yl)hydrazinecarbothioamide

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 1 raw suppliers

Chemical Property of N-Phenyl-2-(phthalazin-1-yl)hydrazinecarbothioamide

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:295.08916661
Heavy Atom Count:21
Complexity:345

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=S)NNC2=NN=CC3=CC=CC=C32

Technology Process of N-Phenyl-2-(phthalazin-1-yl)hydrazinecarbothioamide

There total 4 articles about N-Phenyl-2-(phthalazin-1-yl)hydrazinecarbothioamide 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: 70.0%

: 1044569-46-1
1-hydrazinophthalazine

: 103-72-0
phenyl isothiocyanate

: 61051-54-5
N-phenyl-2-(phthalazin-1-yl)hydrazine-1-carbothioamide

Guidance literature:: In ethanol; for 3h; Reflux;
DOI:10.1016/j.ejmech.2016.07.049

Reference yield:

: 119-67-5
o-carboxybenzaldehyde

: 61051-54-5
N-phenyl-2-(phthalazin-1-yl)hydrazine-1-carbothioamide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate / 1 h

2: trichlorophosphate / 0.03 h

3: hydrazine hydrate / ethanol / 1 h

4: ethanol / 3 h / Reflux

With hydrazine hydrate; trichlorophosphate; In ethanol;
DOI:10.1016/j.ejmech.2016.07.049

Reference yield:

: 119-39-1
phthalazone

: 61051-54-5
N-phenyl-2-(phthalazin-1-yl)hydrazine-1-carbothioamide

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / 0.03 h

2: hydrazine hydrate / ethanol / 1 h

3: ethanol / 3 h / Reflux

With hydrazine hydrate; trichlorophosphate; In ethanol;
DOI:10.1016/j.ejmech.2016.07.049