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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)-

Cinnoline, 7-chloro-

Clc1ccc2c(c1)nncc2 Request for Quotation
Chemical Name: Cinnoline, 7-chloro-
CAS Number: 17404-92-1
Product Number: AG001ZFF(AGN-PC-03BQ9T)
Synonyms:
MDL No:
Molecular Formula: C8H5ClN2
Molecular Weight: 164.5917

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Chlorocinnoline is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. This organic building block has found application in various reactions to access a range of functionalized derivatives. In the realm of medicinal chemistry, 7-Chlorocinnoline serves as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds. Its ability to participate in diverse transformations, such as cross-coupling reactions and C-H functionalization, makes it a valuable tool for building complex molecular architectures. Additionally, the presence of the chloro group in the cinnoline scaffold imparts specific properties that can be further modified for specific applications. Overall, 7-Chlorocinnoline plays a pivotal role in the development of new materials, agrochemicals, and drug molecules, showcasing its significance in modern organic synthesis.