Isopropyl N-(2-ethylphenyl)carbamate

Base Information

Chemical Name:Isopropyl N-(2-ethylphenyl)carbamate
CAS No.:27058-78-2
Molecular Formula:C₁₂H₁₇NO₂
Molecular Weight:207.272
Hs Code.:
European Community (EC) Number:665-927-0

Synonyms:ISOPROPYL N-(2-ETHYLPHENYL)CARBAMATE;AKOS024335580

Suppliers and Price of Isopropyl N-(2-ethylphenyl)carbamate

Supply Marketing:

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

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Chemical Property of Isopropyl N-(2-ethylphenyl)carbamate

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:207.125928785
Heavy Atom Count:15
Complexity:204

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=CC=CC=C1NC(=O)OC(C)C

Technology Process of Isopropyl N-(2-ethylphenyl)carbamate

There total 4 articles about Isopropyl N-(2-ethylphenyl)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:

: 578-54-1
ortho-ethylaniline

: 108-23-6
isopropyl chloroformate

: 27058-78-2
isopropyl (2-ethylphenyl)carbamate

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃;
DOI:10.1016/j.bmcl.2011.09.025

Reference yield:

: 2860-30-2
N-(2-ethylphenyl)formamide

: 27058-78-2
isopropyl (2-ethylphenyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: bis-[(trifluoroacetoxy)iodo]benzene / 1,2-dichloro-ethane / 0.03 h / Molecular sieve; Inert atmosphere

2: 1,2-dichloro-ethane / 1 h / 60 °C / Molecular sieve; Inert atmosphere

With bis-[(trifluoroacetoxy)iodo]benzene; In 1,2-dichloro-ethane;
DOI:10.1039/c4ob00066h