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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)-

4,8-dichloro-6-nitroquinoline-3-carbonitrile

N#Cc1cnc2c(c1Cl)cc(cc2Cl)[N+](=O)[O-] Request for Quotation
Chemical Name: 4,8-dichloro-6-nitroquinoline-3-carbonitrile
CAS Number: 915369-46-9
Product Number: AG00GSN9(AGN-PC-01LXD8)
Synonyms:
MDL No:
Molecular Formula: C10H3Cl2N3O2
Molecular Weight: 268.0557

Identification/Properties

Properties
BP:
456.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
268.053g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
266.96g/mol
Monoisotopic Mass:
266.96g/mol
Topological Polar Surface Area:
82.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
364
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


4,8-Dichloro-6-nitroquinoline-3-carbonitrile is a versatile compound widely used in chemical synthesis. In organic chemistry, this compound serves as a key building block for various complex molecules due to its unique structure and reactivity. Its presence of both electron-withdrawing and electron-donating groups makes it a valuable intermediate for the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. One of the primary applications of 4,8-Dichloro-6-nitroquinoline-3-carbonitrile is in the development of new drug candidates, where it can be modified through various chemical reactions to introduce specific functional groups or target specific biological activities. Additionally, this compound is used in the preparation of dyes and other fine chemicals. Its versatility and importance in chemical synthesis make it a valuable tool for researchers and chemists working in the pharmaceutical and chemical industries.