Cyanamide, (diphenylmethylene)-

Base Information

Chemical Name:Cyanamide, (diphenylmethylene)-
CAS No.:34414-10-3
Molecular Formula:C14H10N2
Molecular Weight:206.247
Hs Code.:
DSSTox Substance ID:DTXSID80350373
Nikkaji Number:J3.327.765B
ChEMBL ID:CHEMBL1608272

Synonyms:Cyanamide, (diphenylmethylene)-;34414-10-3;MLS001174973;SCHEMBL7848715;CHEMBL1608272;DTXSID80350373;HMS1769J03;HMS2911J21;AKOS001015658;SMR000595458;Z56771001

Suppliers and Price of Cyanamide, (diphenylmethylene)-

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 Cyanamide, (diphenylmethylene)-

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:206.084398327
Heavy Atom Count:16
Complexity:265

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=NC#N)C2=CC=CC=C2

Technology Process of Cyanamide, (diphenylmethylene)-

There total 11 articles about Cyanamide, (diphenylmethylene)- 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: 95.0%

: 7677-24-9
trimethylsilyl cyanide

: diphenylmethanone O-(4-(trifluoromethyl)benzoyl) oxime

: 34414-10-3
N-(diphenylmethylene)cyanamide

Guidance literature:: With 1,10-Phenanthroline; tetrakis(acetonitrile)copper(I)tetrafluoroborate; fac-tris(2-(4'-tert-butyl)phenylpyridine)iridium(III); In chlorobenzene; at 25 ℃; for 12h; Solvent; Reagent/catalyst; Catalytic behavior; Inert atmosphere; Sealed tube; Irradiation;
DOI:10.1021/acs.orglett.0c02659