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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)-

4H-Pyrrolo[3,2,1-ij]quinoline, 5,6-dihydro-

c1cc2CCCn3c2c(c1)cc3 Request for Quotation
Chemical Name: 4H-Pyrrolo[3,2,1-ij]quinoline, 5,6-dihydro-
CAS Number: 5840-01-7
Product Number: AG003M9Z(AGN-PC-00Q1XG)
Synonyms:
MDL No:
Molecular Formula: C11H11N
Molecular Weight: 157.2117

Identification/Properties

Properties
MP:
80-81°C
BP:
318.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
157.216g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
157.089g/mol
Monoisotopic Mass:
157.089g/mol
Topological Polar Surface Area:
4.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
178
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


5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline, also known as $name$, features a unique molecular structure that lends itself to various applications in chemical synthesis. This compound serves as a valuable building block in the creation of complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its fused ring system provides a versatile platform for the construction of diverse molecular frameworks, making it a valuable intermediate in the synthesis of biologically active compounds. The presence of multiple reactive sites enables selective functionalization, allowing chemists to tailor the molecule for specific applications. In particular, $name$ is utilized in the synthesis of heterocyclic compounds and natural product derivatives, where its structural features play a crucial role in the formation of intricate chemical structures. Its use in multistep synthesis cascades allows for efficient access to target molecules with high structural diversity. Overall, the application of 5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline in chemical synthesis showcases its importance as a versatile building block for the construction of complex organic molecules with potential utility across various industries.