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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, 3,4-diethyl-

CCc1c[nH]cc1CC Request for Quotation
Chemical Name: 1H-Pyrrole, 3,4-diethyl-
CAS Number: 16200-52-5
Product Number: AG001SN2(AGN-PC-0NCNOJ)
Synonyms:
MDL No: MFCD08062571
Molecular Formula: C8H13N
Molecular Weight: 123.1955

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
123.199g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
123.105g/mol
Monoisotopic Mass:
123.105g/mol
Topological Polar Surface Area:
15.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
70.6
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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


3,4-Diethyl-1H-pyrrole is a versatile compound widely utilized in chemical synthesis. This heterocyclic compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. In chemical synthesis, 3,4-Diethyl-1H-pyrrole serves as a key building block for the construction of complex molecules and organic frameworks. Its presence often imparts desirable properties such as improved stability, enhanced reactivity, and specific stereochemistry to the final products. By incorporating 3,4-Diethyl-1H-pyrrole into synthetic pathways, chemists can access a diverse array of functionalized compounds with valuable applications in drug discovery, materials science, and chemical research.