1-Benzyl-3-(p-tolyl)urea

Base Information

Chemical Name:1-Benzyl-3-(p-tolyl)urea
CAS No.:13143-43-6
Molecular Formula:C₁₅H₁₆N₂O
Molecular Weight:240.305
Hs Code.:
European Community (EC) Number:667-325-3
Nikkaji Number:J281.859K
Mol file:13143-43-6.mol

Synonyms:1-Benzyl-3-(p-tolyl)urea;SCHEMBL5853157;N-benzyl-N'-(4-methylphenyl)urea;AKOS002979809

Suppliers and Price of 1-Benzyl-3-(p-tolyl)urea

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

Sigma-Aldrich
1-BENZYL-3-(P-TOLYL)UREA AldrichCPR
250mg
$ 57.00

Total 2 raw suppliers

Chemical Property of 1-Benzyl-3-(p-tolyl)urea

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:240.126263138
Heavy Atom Count:18
Complexity:253

Purity/Quality:

98%,99%, ^*data from raw suppliers

1-BENZYL-3-(P-TOLYL)UREA AldrichCPR ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)NC(=O)NCC2=CC=CC=C2

Technology Process of 1-Benzyl-3-(p-tolyl)urea

There total 23 articles about 1-Benzyl-3-(p-tolyl)urea 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: 99.0%

: 622-58-2,374675-64-6
p-Tolylisocyanate

: 100-46-9
benzylamine

: 13143-43-6
1-(4-phenylmethyl)-3-(4-methylphenyl)urea

Guidance literature:: With C₆₄H₅₂CaN₆; In neat (no solvent); at 60 ℃; for 12h; Schlenk technique; Glovebox; Inert atmosphere;
DOI:10.1039/d0nj01509a

Reference yield: 98.0%

: (4-methylphenyl)carbamic acid

: 100-46-9
benzylamine

: 13143-43-6
1-(4-phenylmethyl)-3-(4-methylphenyl)urea

Guidance literature:: With trichloroisocyanuric acid; triphenylphosphine; In 1,4-dioxane; at 80 ℃; for 3h;
DOI:10.1080/10426507.2015.1085038

Reference yield: 93.0%

: 102276-50-6
β,β,β-Trichloroethyl Benzylaminoformate

: 106-49-0,12221-03-3
p-toluidine

: 13143-43-6
1-(4-phenylmethyl)-3-(4-methylphenyl)urea

Guidance literature:: p-toluidine; With bis(trimethylaluminum)–1,4-diazabicyclo[2.2.2]octane adduct; In toluene; at 40 ℃; for 0.5h;

β,β,β-Trichloroethyl Benzylaminoformate; In toluene; for 3h;
DOI:10.1071/CH15675