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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)-

6,8-dichloro-2-methylquinolin-4-amine

Clc1cc(Cl)c2c(c1)c(N)cc(n2)C Request for Quotation
Chemical Name: 6,8-dichloro-2-methylquinolin-4-amine
CAS Number: 917562-01-7
Product Number: AG006DQ1(AGN-PC-01A9FT)
Synonyms:
MDL No:
Molecular Formula: C10H8Cl2N2
Molecular Weight: 227.0899

Identification/Properties

Computed Properties
Molecular Weight:
227.088g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
226.006g/mol
Monoisotopic Mass:
226.006g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
212
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,8-Dichloro-2-methylquinolin-4-amine is a versatile chemical compound widely used in chemical synthesis processes. Its unique structure and reactivity make it an essential building block in the production of various organic compounds. In chemical synthesis, this compound serves as a key intermediate in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to undergo selective functional group transformations allows for the successful modification and diversification of molecular structures, enabling the synthesis of complex molecules with high efficiency and precision. Moreover, its halogen substituents provide opportunities for further derivatization, making it a valuable tool for organic chemists seeking to develop new chemical entities with enhanced properties and functionalities.