4-chlorophenyl N-phenethylcarbamate

Base Information

Chemical Name:4-chlorophenyl N-phenethylcarbamate
CAS No.:132906-01-5
Molecular Formula:C₁₅H₁₄ClNO₂
Molecular Weight:275.735
Hs Code.:
DSSTox Substance ID:DTXSID801324326
Nikkaji Number:J1.395.058J
Pharos Ligand ID:MRKY1922T1T1
ChEMBL ID:CHEMBL1579150

Synonyms:MLS000851155;4-chlorophenyl N-phenethylcarbamate;SMR000457398;(4-chlorophenyl) N-(2-phenylethyl)carbamate;132906-01-5;Maybridge3_000608;CHEMBL1579150;p-Chlorophenyl phenethylcarbamate;BDBM96733;cid_2802347;DTXSID801324326;HMS1432L14;HMS2782G15;CCG-54132;IDI1_011995;N-phenethylcarbamic acid (4-chlorophenyl) ester;SR-01000643251-1;N-(2-phenylethyl)carbamic acid (4-chlorophenyl) ester

Suppliers and Price of 4-chlorophenyl N-phenethylcarbamate

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 4-chlorophenyl N-phenethylcarbamate

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:275.0713064
Heavy Atom Count:19
Complexity:271

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CCNC(=O)OC2=CC=C(C=C2)Cl

Technology Process of 4-chlorophenyl N-phenethylcarbamate

There total 3 articles about 4-chlorophenyl N-phenethylcarbamate 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: 93.0%

: 1943-82-4
phenethyl isocyanate

: 106-48-9,82344-39-6
4-chloro-phenol

: 132906-01-5
4-chlorophenyl (2-phenylethyl)carbamate

Guidance literature:: With triethylamine; In acetonitrile; at 20 ℃; for 2.25h;
DOI:10.1016/j.bioorg.2018.07.017

Reference yield: 66.5%

: 132905-83-0
Carbonic acid chloromethyl ester 4-chloro-phenyl ester

: 64-04-0
phenethylamine

: 132906-01-5
4-chlorophenyl (2-phenylethyl)carbamate

Guidance literature:: In benzene; a.) RT, 1 h, b.) reflux, 1 h;

Reference yield:

: 106-48-9,82344-39-6
4-chloro-phenol

: 132906-01-5
4-chlorophenyl (2-phenylethyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 72.6 percent / Et₃N / CH₂Cl₂ / 1.67 h / 5 °C

2: 66.5 percent / benzene / a.) RT, 1 h, b.) reflux, 1 h

With triethylamine; In dichloromethane; benzene;