N-[(E)-amino(1,3-benzothiazol-2-ylamino)methylidene]-3-chlorobenzamide

Base Information

Chemical Name:N-[(E)-amino(1,3-benzothiazol-2-ylamino)methylidene]-3-chlorobenzamide
CAS No.:6260-33-9
Molecular Formula:C₆H₁₁O₃P
Molecular Weight:162.125
Hs Code.:
DSSTox Substance ID:DTXSID60430586

Synonyms:ChemDiv3_004617;6260-33-9;SCHEMBL13522371;DTXSID60430586;HMS1486B19;STK028640;AKOS001654072;IDI1_022527;N-[(E)-amino(1,3-benzothiazol-2-ylamino)methylidene]-3-chlorobenzamide;N-[(E)-AMINO[(1,3-BENZOTHIAZOL-2-YL)AMINO]METHYLIDENE]-3-CHLOROBENZAMIDE

Suppliers and Price of N-[(E)-amino(1,3-benzothiazol-2-ylamino)methylidene]-3-chlorobenzamide

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 0 raw suppliers

Chemical Property of N-[(E)-amino(1,3-benzothiazol-2-ylamino)methylidene]-3-chlorobenzamide

Chemical Property:

Vapor Pressure:1.81E-11mmHg at 25°C
Boiling Point:533.7°C at 760 mmHg
Flash Point:276.6°C
Density:1.49g/cm³
XLogP3:4.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:330.0342099
Heavy Atom Count:22
Complexity:447

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)N=C(S2)N=C(N)NC(=O)C3=CC(=CC=C3)Cl
Isomeric SMILES:C1=CC=C2C(=C1)N=C(S2)/N=C(\N)/NC(=O)C3=CC(=CC=C3)Cl

Technology Process of N-[(E)-amino(1,3-benzothiazol-2-ylamino)methylidene]-3-chlorobenzamide

There total 1 articles about N-[(E)-amino(1,3-benzothiazol-2-ylamino)methylidene]-3-chlorobenzamide 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: