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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Pyrrole, 2,5-diethyl-

CCc1ccc([nH]1)CC Request for Quotation
Chemical Name: 1H-Pyrrole, 2,5-diethyl-
CAS Number: 766-95-0
Product Number: AG005AJN(AGN-PC-0JMOYT)
Synonyms:
MDL No:
Molecular Formula: C8H13N
Molecular Weight: 123.1955

Identification/Properties

Properties
BP:
189.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Diethyl-1H-pyrrole is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural characteristics. This compound is commonly employed as a building block in the synthesis of various organic molecules, especially in the development of pharmaceuticals, agrochemicals, and materials science.In organic synthesis, 2,5-Diethyl-1H-pyrrole serves as a key intermediate for the construction of complex molecular structures. Its heterocyclic nature and electron-rich pyrrole ring make it a valuable starting material for the synthesis of biologically active compounds. By functionalizing the diethyl substituents or the pyrrole ring itself, chemists can introduce specific functional groups or modify the compound's properties to tailor it for a particular application.Additionally, 2,5-Diethyl-1H-pyrrole is known for its role in the preparation of ligands for transition metal catalysis. The nitrogen atom in the pyrrole ring can coordinate with metal ions, allowing the compound to act as a chelating agent in catalytic processes. This capability opens up opportunities for the development of novel catalytic systems with enhanced efficiency and selectivity.Overall, the application of 2,5-Diethyl-1H-pyrrole in chemical synthesis showcases its importance as a valuable synthetic building block with wide-ranging potential in the field of organic chemistry.