2-Cyanophenyl (4-chlorophenyl)carbamate

Base Information

Chemical Name:2-Cyanophenyl (4-chlorophenyl)carbamate
CAS No.:88220-36-4
Molecular Formula:C14H9ClN2O2
Molecular Weight:272.691
Hs Code.:
DSSTox Substance ID:DTXSID80521622
Wikidata:Q82386198

Synonyms:2-Cyanophenyl (4-chlorophenyl)carbamate;88220-36-4;DTXSID80521622

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-Cyanophenyl (4-chlorophenyl)carbamate

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:272.0352552
Heavy Atom Count:19
Complexity:358

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C#N)OC(=O)NC2=CC=C(C=C2)Cl

Technology Process of 2-Cyanophenyl (4-chlorophenyl)carbamate

There total 1 articles about 2-Cyanophenyl (4-chlorophenyl)carbamate 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: 91.0%

: 611-20-1
salicylonitrile

: 104-12-1
p-chlorphenylisocyanate

: 88220-36-4
2-<(4-chlorophenyl)aminocarbonyloxy>benzonitrile

Guidance literature:: With triethylamine; In diethyl ether; for 0.0833333h;

Reference yield: 75.0%

: 88220-36-4
2-<(4-chlorophenyl)aminocarbonyloxy>benzonitrile

: 88220-44-4
4-<(4-chlorophenyl)amino>-2H-1,3-benzoxazin-2-one

Guidance literature:: With triethylamine; In toluene; for 46h; Heating;

Reference yield:

: 88220-36-4
2-<(4-chlorophenyl)aminocarbonyloxy>benzonitrile

: 140-38-5
N-(4-chlorophenyl)urea

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / triethylamine / benzene / 69 h / Heating

2: 0.050 g / conc. HCl / ethanol / 7 h / Heating

With hydrogenchloride; triethylamine; In ethanol; benzene;