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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)-

Benzo[c]cinnoline

c1ccc2c(c1)c1ccccc1nn2 Request for Quotation
Chemical Name: Benzo[c]cinnoline
CAS Number: 230-17-1
Product Number: AG002LTY(AGN-PC-0JK8X8)
Synonyms:
MDL No:
Molecular Formula: C12H8N2
Molecular Weight: 180.2053

Identification/Properties

Properties
MP:
156-159℃
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
180.21g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
180.069g/mol
Monoisotopic Mass:
180.069g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
183
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-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzo[c]cinnoline is a highly versatile compound that finds widespread application in chemical synthesis. It serves as a valuable building block in the creation of various organic molecules due to its unique structural properties and reactivity. In synthesis, Benzo[c]cinnoline acts as a key intermediate for the production of diverse compounds such as pharmaceuticals, agrochemicals, and materials. Its aromatic ring system and potential for functional group manipulation make it an ideal starting material for the formation of intricate molecular structures. Additionally, Benzo[c]cinnoline can undergo various reactions, including substitution, oxidation, and reduction, allowing for the customization of its chemical properties to suit specific synthesis needs. Its broad utility in organic synthesis makes Benzo[c]cinnoline a valuable tool for chemists seeking to access complex and biologically active compounds efficiently and effectively.