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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)-

3-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-1H-pyrrolo[2,3-b]pyridine

CN1CCC(=CC1)c1c[nH]c2c1cccn2 Request for Quotation
Chemical Name: 3-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-1H-pyrrolo[2,3-b]pyridine
CAS Number: 325975-67-5
Product Number: AG00CMR6(AGN-PC-0NHRUH)
Synonyms:
MDL No:
Molecular Formula: C13H15N3
Molecular Weight: 213.2783

Identification/Properties

Computed Properties
Molecular Weight:
213.284g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
213.127g/mol
Monoisotopic Mass:
213.127g/mol
Topological Polar Surface Area:
31.9A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
287
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-pyrrolo[2,3-b]pyridine, also known as $name$, plays a significant role in chemical synthesis as a versatile building block. Its unique structure, combining a tetrahydropyridine moiety with a pyrrolopyridine ring system, imparts valuable properties that make it a valuable intermediate in the synthesis of various organic compounds.In chemical synthesis, $name$ is commonly used as a key starting material for the preparation of diverse target molecules with complex structures. It can undergo various reactions such as functional group modifications, cross-coupling reactions, and ring formations to create novel compounds with potential applications in pharmaceuticals, agrochemicals, materials science, and other industries.The presence of the tetrahydropyridine group in $name$ provides a versatile platform for introducing different substituents and functional groups, allowing chemists to tailor the compound's properties for specific synthetic applications. Furthermore, the fused pyrrolopyridine ring system enhances the structural diversity and conformational flexibility of the final products, making it an attractive scaffold for designing biologically active molecules with improved potency and selectivity.Overall, the strategic incorporation of 3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-pyrrolo[2,3-b]pyridine in chemical synthesis enables the efficient construction of complex organic molecules with tailored properties, thus contributing to the advancement of drug discovery, materials development, and other fields of research.