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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)-

N-methyl-1-(1H-pyrrol-2-yl)ethanamine

CNCc1cccn1C Request for Quotation
Chemical Name: N-methyl-1-(1H-pyrrol-2-yl)ethanamine
CAS Number: 26052-09-5
Product Number: AG002RJD(AGN-PC-09RRZ4)
Synonyms:
MDL No:
Molecular Formula: C7H12N2
Molecular Weight: 124.1836

Identification/Properties

Computed Properties
Molecular Weight:
124.18g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
124.100048g/mol
Monoisotopic Mass:
124.100048g/mol
Topological Polar Surface Area:
17Ų
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
83
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


N-Methyl-1-(1H-pyrrol-2-yl)ethanamine is a versatile compound that finds wide application in chemical synthesis as a key building block. It plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structure and reactivity. In organic synthesis, it serves as a valuable intermediate for the preparation of heterocyclic compounds and complex organic molecules. Its presence in a reaction cascade can facilitate diverse transformations, enabling the formation of novel compounds with potential biological or industrial significance. The controlled and selective functionalization of N-Methyl-1-(1H-pyrrol-2-yl)ethanamine allows for the design and optimization of synthetic routes towards target molecules, making it a valuable asset in the field of chemical synthesis.