1H-Pyrrole-2-carboxylic acid, 5-(4-fluorophenyl)-, ethyl ester

Base Information

Chemical Name:1H-Pyrrole-2-carboxylic acid, 5-(4-fluorophenyl)-, ethyl ester
CAS No.:143446-15-5
Molecular Formula:C13H12FNO2
Molecular Weight:233.242
Hs Code.:
DSSTox Substance ID:DTXSID10434554
Nikkaji Number:J495.844F
Wikidata:Q82249010
Mol file:143446-15-5.mol

Synonyms:1H-Pyrrole-2-carboxylic acid, 5-(4-fluorophenyl)-, ethyl ester;143446-15-5;DTXSID10434554;5-(4-Fluorophenyl)-1H-pyrrole-2-carboxylic acid ethyl ester

Suppliers and Price of 1H-Pyrrole-2-carboxylic acid, 5-(4-fluorophenyl)-, ethyl ester

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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 1H-Pyrrole-2-carboxylic acid, 5-(4-fluorophenyl)-, ethyl ester

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:233.08520679
Heavy Atom Count:17
Complexity:264

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=CC=C(N1)C2=CC=C(C=C2)F

Technology Process of 1H-Pyrrole-2-carboxylic acid, 5-(4-fluorophenyl)-, ethyl ester

There total 7 articles about 1H-Pyrrole-2-carboxylic acid, 5-(4-fluorophenyl)-, ethyl ester 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: 40.0%

: (Z)-3-chloro-3-(4-fluorophenyl)-prop-2-ene-1-ylidene-dimethyliminium perchlorat

: 459-73-4
GlyOEt*HCl

: 143446-15-5
2-carbethoxy-5-(4-fluorophenyl)pyrrole

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; Heating;
DOI:10.1021/jo00046a033

Reference yield:

: 144978-35-8,144978-12-1,251924-83-1
(S)-ethyl N-tert-butoxycarbonylpyroglutamate

: 143446-15-5
2-carbethoxy-5-(4-fluorophenyl)pyrrole

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / tetrahydrofuran / -40 °C

2: 93 percent / TFA / CH₂Cl₂

3: NBS, AIBN / CCl₄

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); trifluoroacetic acid; In tetrahydrofuran; tetrachloromethane; dichloromethane;
DOI:10.1016/S0040-4039(00)73741-5

Reference yield:

: 352-13-6
4-flourophenylmagnesium bromide

: 143446-15-5
2-carbethoxy-5-(4-fluorophenyl)pyrrole

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / tetrahydrofuran / -40 °C

2: 93 percent / TFA / CH₂Cl₂

3: NBS, AIBN / CCl₄

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); trifluoroacetic acid; In tetrahydrofuran; tetrachloromethane; dichloromethane;
DOI:10.1016/S0040-4039(00)73741-5