2-Cyanophenyl (3-chloropropyl)carbamate

Base Information

Chemical Name:2-Cyanophenyl (3-chloropropyl)carbamate
CAS No.:88220-38-6
Molecular Formula:C11H11ClN2O2
Molecular Weight:238.674
Hs Code.:
DSSTox Substance ID:DTXSID80521627
Wikidata:Q82386206

Synonyms:2-Cyanophenyl (3-chloropropyl)carbamate;88220-38-6;DTXSID80521627

Suppliers and Price of 2-Cyanophenyl (3-chloropropyl)carbamate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Cyanophenyl (3-chloropropyl)carbamate

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:238.0509053
Heavy Atom Count:16
Complexity:274

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C#N)OC(=O)NCCCCl

Technology Process of 2-Cyanophenyl (3-chloropropyl)carbamate

There total 1 articles about 2-Cyanophenyl (3-chloropropyl)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: 92.0%

: 13010-19-0
3-Chloropropyl isocyanate

: 611-20-1
salicylonitrile

: 88220-38-6
2-<(3-chloropropyl)aminocarbonyloxy>benzonitrile

Guidance literature:: With triethylamine; In diethyl ether; for 2h; Ambient temperature;

Reference yield:

: 88220-38-6
2-<(3-chloropropyl)aminocarbonyloxy>benzonitrile

: 65739-64-2
1,4,5,6-tetrahydro-2-(2-hydroxyphenyl)pyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / triethylamine / toluene / 18 h / Heating

2: 58 percent / 10percent aq. KOH / 18 h / Ambient temperature; neutralized with 2N HCl

With potassium hydroxide; triethylamine; In toluene;