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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-Quinolinemethanamine

NCc1ccc2c(c1)cccn2 Request for Quotation
Chemical Name: 6-Quinolinemethanamine
CAS Number: 99071-54-2
Product Number: AG0034BN(AGN-PC-0K6A5O)
Synonyms:
MDL No: MFCD02853688
Molecular Formula: C10H10N2
Molecular Weight: 158.1998

Identification/Properties

Properties
BP:
314.7 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Refractive Index:
1.6410-1.6450
Computed Properties
Molecular Weight:
158.204g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
158.084g/mol
Monoisotopic Mass:
158.084g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
147
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Quinolinemethanamine is a versatile chemical compound commonly used in chemical synthesis for its unique reactivity and functional group compatibility. It serves as a key intermediate in the preparation of various organic compounds due to its ability to undergo a wide range of transformations.In organic synthesis, 6-Quinolinemethanamine can be utilized as a building block in the construction of complex molecules such as pharmaceuticals, agrochemicals, and materials. It can participate in numerous reactions including nucleophilic addition, acylation, alkylation, and condensation, allowing for the introduction of diverse functional groups into the final product.The presence of the quinoline moiety in 6-Quinolinemethanamine imparts specific properties to the molecules it is incorporated into, making it valuable for the design and preparation of compounds with desired chemical and biological activities. Its use in the synthesis of heterocyclic structures further expands its applicability in medicinal chemistry and drug discovery efforts.Overall, 6-Quinolinemethanamine plays a crucial role in chemical synthesis by enabling the efficient and strategic assembly of complex organic molecules with diverse applications across different fields of science and industry.