2-(3-Ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)acetic acid ethyl ester

Base Information

Chemical Name:2-(3-Ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)acetic acid ethyl ester
CAS No.:74007-93-5
Molecular Formula:C₁₃H₂₀N₂O₃S
Molecular Weight:284.379
Hs Code.:

Synonyms:BRN 1009906;2-(3-Ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)acetic acid ethyl ester;Acetic acid, 2-(3-ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)-, ethyl ester;delta(sup 2,alpha)-Thiazolidineacetic acid, 3-ethyl-4-oxo-5-pyrrolidin-1-yl-, ethyl ester;74007-93-5;LS-151096;Acetic acid, [3-ethyl-4-oxo-5-(1-pyrrolidinyl)-2-thiazolidinylidene]-, ethyl ester

Suppliers and Price of 2-(3-Ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)acetic acid ethyl ester

Supply Marketing:

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

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Chemical Property of 2-(3-Ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)acetic acid ethyl ester

Chemical Property:

Vapor Pressure:3.32E-08mmHg at 25°C
Boiling Point:447.6°C at 760 mmHg
Flash Point:224.5°C
Density:1.289g/cm³
XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:284.11946368
Heavy Atom Count:19
Complexity:391

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN1C(=CC(=O)OCC)SC(C1=O)N2CCCC2
Isomeric SMILES:CCN1/C(=C/C(=O)OCC)/SC(C1=O)N2CCCC2

Technology Process of 2-(3-Ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)acetic acid ethyl ester

There total 2 articles about 2-(3-Ethyl-4-oxo-5-pyrrolidin-1-yl-2-thiazolidinylidene)acetic acid 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:

: 24146-36-9
2-ethoxycarbonylmethylidene-4,5-dihydro-4-thiazolinone

: 74007-93-5
3-Ethyl-5-pyrrolidino-2-ethoxycarbonylmethylen-thiazolidon-(4)

Guidance literature:: Multi-step reaction with 2 steps

1: (i) Na₂CO₃, aq. EtOH, (ii) /BRN= 1209714/

2: (i) Br₂, CHCl₃, (ii) /BRN= 102395/, benzene