1. Home
  2. 2-(2-quinolin-3-ylpyridin-4-yl)-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one;hydrate

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

2-(2-quinolin-3-ylpyridin-4-yl)-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one;hydrate

O=C1NCCc2c1cc([nH]2)c1ccnc(c1)c1cnc2c(c1)cccc2.O Request for Quotation
Chemical Name: 2-(2-quinolin-3-ylpyridin-4-yl)-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one;hydrate
CAS Number: 1186648-22-5
Product Number: AG0097FQ(AGN-PC-04ZXUE)
Synonyms:
MDL No:
Molecular Formula: C21H18N4O2
Molecular Weight: 358.3932

Identification/Properties

Computed Properties
Molecular Weight:
358.401g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
358.143g/mol
Monoisotopic Mass:
358.143g/mol
Topological Polar Surface Area:
71.7A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
526
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The compound 2-(2-(Quinolin-3-yl)pyridin-4-yl)-6,7-dihydro-1H-pyrrolo[3,2-c]pyridin-4(5H)-one hydrate, also known as $name$, serves as a versatile building block in chemical synthesis processes. Its unique structure and functional groups make it a valuable intermediate in the preparation of various organic compounds. In particular, $name$ can be utilized in the synthesis of heterocyclic compounds, pharmaceuticals, and agrochemicals. Its presence enables the introduction of the quinoline and pyridine moieties into target molecules, allowing for the customization of chemical structures for specific applications. With its strategic placement of reactive sites, $name$ offers chemists a reliable tool for creating complex molecular architectures with precise control over regioselectivity and functional group compatibility. By incorporating 2-(2-(Quinolin-3-yl)pyridin-4-yl)-6,7-dihydro-1H-pyrrolo[3,2-c]pyridin-4(5H)-one hydrate into synthetic routes, researchers can efficiently access novel compounds with enhanced properties and tailored functionalities.