Recommended Products
Quality Level
Assay
97%
mp
100-104 °C (lit.)
SMILES string
CCC1=C(C)CNC1=O
InChI
1S/C7H11NO/c1-3-6-5(2)4-8-7(6)9/h3-4H2,1-2H3,(H,8,9)
InChI key
YCTNTSVMJWIYTQ-UHFFFAOYSA-N
Related Categories
General description
3-Ethyl-4-methyl-3-pyrrolin-2-one, a five-membered α,β-unsaturated lactam derivative, has various applications in medicinal chemistry. It can be synthesized by employing following as starting materials:
- allylamine, via palladium(II)-assisted cyclization
- 4-methoxybenzylamine, via a ring-closing-metathesis strategy
- 3-ethyl-1-(4-methoxybenzyl)-4-methyl-1,5-dihydro-2H-pyrrol-2- one
Application
3-Ethyl-4-methyl-3-pyrrolin-2-one (3-Ethyl-4-methyl-1,5-dihydro-2H-pyrrol-2-one) may be employed as a precursor for the synthesis of glimepiride (antidiabetic drug) and its derivatives (sulfonylurea drugs). It may also be employed for the preparation of 2-ethyl-3-methyl-(10H)-
dipyrrin-1-one.
dipyrrin-1-one.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis of 3-Ethyl-4-methyl-1, 5-dihydro-2H-pyrrol-2-one by Novel Palladium (II)-Catalyzed Cyclization and Ring-Closing Metathesis.
Synthesis, 47(07), 955-960 (2015)
Molecular recognition studies with a simple dipyrrinone.
Tetrahedron, 63(52), 12994-12999 (2007)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service