Ethyl 4-(3-chlorophenoxy)butanoate

Base Information

Chemical Name:Ethyl 4-(3-chlorophenoxy)butanoate
CAS No.:37483-53-7
Molecular Formula:C12H15ClO3
Molecular Weight:242.702
Hs Code.:2918990090
DSSTox Substance ID:DTXSID60190931
Wikidata:Q83063397
Mol file:37483-53-7.mol

Synonyms:37483-53-7;ethyl 4-(3-chlorophenoxy)butanoate;4-(3-CHLORO-PHENOXY)-BUTYRIC ACID ETHYL ESTER;Ethyl 4-(3-chlorophenoxy)butyrate;4-(3-Chlorophenoxy)butanoic acid ethyl ester;BRN 1973606;BUTANOIC ACID, 4-(3-CHLOROPHENOXY)-, ETHYL ESTER;DTXSID60190931;MFCD01741115;AKOS005215915;SB36902;LS-46158;CS-0340406

Suppliers and Price of Ethyl 4-(3-chlorophenoxy)butanoate

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

J&W Pharmlab
4-(3-Chloro-phenoxy)-butyricacidethylester 96%
5g
$ 3998.00

Crysdot
Ethyl4-(3-chlorophenoxy)butanoate 95+%
1g
$ 402.00

American Custom Chemicals Corporation
4-(3-CHLORO-PHENOXY)-BUTYRIC ACID ETHYL ESTER 96.00%
5MG
$ 495.53

Alichem
Ethyl4-(3-chlorophenoxy)butanoate
1g
$ 324.72

Total 7 raw suppliers

Chemical Property of Ethyl 4-(3-chlorophenoxy)butanoate

Chemical Property:

Vapor Pressure:8.76E-05mmHg at 25°C
Boiling Point:340.2°Cat760mmHg
Flash Point:135.1°C
PSA：35.53000
Density:1.148g/cm³
LogP:3.06210
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:242.0709720
Heavy Atom Count:16
Complexity:208

Purity/Quality:

97% ^*data from raw suppliers

4-(3-Chloro-phenoxy)-butyricacidethylester 96% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)CCCOC1=CC(=CC=C1)Cl

Technology Process of Ethyl 4-(3-chlorophenoxy)butanoate

There total 3 articles about Ethyl 4-(3-chlorophenoxy)butanoate 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: 87.0%

: 108-43-0
3-monochlorophenol

: 2969-81-5
Ethyl 4-bromobutyrate

: 37483-53-7
ethyl 4-(3-chlorophenoxy)butanoate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 90 ℃; for 16h;
DOI:10.1021/acs.jmedchem.9b00462

Reference yield: 72.0%

: 64-17-5
ethanol

: 201230-82-2
carbon monoxide

: 24824-86-0
1-(allyloxy)-3-chlorobenzene

: 37483-53-7
ethyl 4-(3-chlorophenoxy)butanoate

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2-methyl-but-2-ene; hydrogen; 1,4-di(diphenylphosphino)-butane; In chloroform; at 120 ℃; for 36h; under 31029.7 Torr; regioselective reaction; Schlenk technique; Inert atmosphere; Autoclave;
DOI:10.1021/acs.joc.6b00522