Benzamide, N-(iminophenylmethyl)-4-methyl-

Base Information

Chemical Name:Benzamide, N-(iminophenylmethyl)-4-methyl-
CAS No.:68167-55-5
Molecular Formula:C15H14N2O
Molecular Weight:238.289
Hs Code.:
DSSTox Substance ID:DTXSID50443786
Nikkaji Number:J1.213.756G

Synonyms:Benzamide, N-(iminophenylmethyl)-4-methyl-;68167-55-5;DTXSID50443786;N-(alpha-Iminobenzyl)-4-methylbenzamide

Suppliers and Price of Benzamide, N-(iminophenylmethyl)-4-methyl-

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 Benzamide, N-(iminophenylmethyl)-4-methyl-

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:238.110613074
Heavy Atom Count:18
Complexity:311

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=O)N=C(C2=CC=CC=C2)N

Technology Process of Benzamide, N-(iminophenylmethyl)-4-methyl-

There total 2 articles about Benzamide, N-(iminophenylmethyl)-4-methyl- 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: 78.0%

: 1670-14-0
benzamidine monohydrochloride

: 874-60-2
4-methyl-benzoyl chloride

: 68167-55-5
N-(4-methylbenzoyl)benzamidine

Guidance literature:: DOI:10.1021/jo952106w

Reference yield:

: 1670-14-0
benzamidine monohydrochloride

: 99-94-5
p-Toluic acid

: 68167-55-5
benzimidoyl-p-toluoyl-amine

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 3h;
DOI:10.1016/j.tet.2018.07.036

Reference yield: 99.0%

: 68167-55-5
benzimidoyl-p-toluoyl-amine

: 16112-24-6
3-phenyl-5-(p-tolyl)-1,2,4-oxadiazole

Guidance literature:: With N-Bromosuccinimide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In ethyl acetate; at 20 ℃; for 0.166667h; Green chemistry;
DOI:10.1016/j.tet.2018.07.036