N-[(Anilinothiocarbamoylamino)thiocarbamoyl]benzamide

Base Information

Chemical Name:N-[(Anilinothiocarbamoylamino)thiocarbamoyl]benzamide
CAS No.:33949-90-5
Molecular Formula:C₁₅H₁₅N₅OS₂
Molecular Weight:345.449
Hs Code.:
DSSTox Substance ID:DTXSID70407668
NSC Number:176373

Synonyms:33949-90-5;N-[(ANILINOTHIOCARBAMOYLAMINO)THIOCARBAMOYL]BENZAMIDE;NSC176373;DTXSID70407668;NSC-176373

Suppliers and Price of N-[(Anilinothiocarbamoylamino)thiocarbamoyl]benzamide

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 5 raw suppliers

Chemical Property of N-[(Anilinothiocarbamoylamino)thiocarbamoyl]benzamide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.401g/cm³
XLogP3:3.8
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:345.07180247
Heavy Atom Count:23
Complexity:420

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)C(=O)NC(=S)NNC(=S)NNC2=CC=CC=C2

Technology Process of N-[(Anilinothiocarbamoylamino)thiocarbamoyl]benzamide

There total 1 articles about N-[(Anilinothiocarbamoylamino)thiocarbamoyl]benzamide 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:

: 33949-90-5
4-benzoyl-1-(N'-phenyl-hydrazinothiocarbonyl)-thiosemicarbazide

Guidance literature:: Phenylthiocarbonhydrazid, Benzoylthiocyanat (S.2936);
DOI:10.1039/j39710002932

Reference yield:

: 33949-90-5
4-benzoyl-1-(N'-phenyl-hydrazinothiocarbonyl)-thiosemicarbazide

: 33949-92-7
N-(5-phenylazo-[1,3,4]thiadiazol-2-yl)-benzamide

Guidance literature:: With hydrogenchloride; dihydrogen peroxide; In ethanol; Heating;
DOI:10.1039/j39710002932

Reference yield:

: 33949-90-5
4-benzoyl-1-(N'-phenyl-hydrazinothiocarbonyl)-thiosemicarbazide

: 34240-11-4
N-(5-methanesulfonyl-[1,3,4]thiadiazol-2-yl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: methanol / Heating

2: aq. H₂O₂, AcOH

With dihydrogen peroxide; acetic acid; In methanol;
DOI:10.1039/j39710002932