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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)-

quinolin-3-ylmethanamine;dihydrochloride

NCc1cnc2c(c1)cccc2.Cl.Cl Request for Quotation
Chemical Name: quinolin-3-ylmethanamine;dihydrochloride
CAS Number: 31842-22-5
Product Number: AG00CKZJ(AGN-PC-07HCSJ)
Synonyms:
MDL No:
Molecular Formula: C10H12Cl2N2
Molecular Weight: 231.1217

Identification/Properties

Computed Properties
Molecular Weight:
231.12g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
230.038g/mol
Monoisotopic Mass:
230.038g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
14
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:
3
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


Quinolin-3-ylmethanamine dihydrochloride, also known as $name$, is a powerful agent frequently utilized in chemical synthesis processes. This compound serves as a versatile building block in the creation of various complex organic molecules. Its unique structure and reactivity make it an essential tool in the development of pharmaceuticals, agrochemicals, and other specialized chemicals.One critical application of $name$ lies in its role as a key intermediate in the synthesis of heterocyclic compounds. By acting as a precursor in diverse chemical reactions, it enables the formation of intricate structures that are crucial in the pharmaceutical industry. Furthermore, the presence of the quinoline moiety in $name$ enhances its utility in medicinal chemistry, facilitating the design and production of novel drug candidates.Additionally, $name$ plays a vital function in the creation of ligands for catalytic processes. Its ability to participate in various coupling reactions and functional group transformations makes it an invaluable tool for the development of catalysts used in organic synthesis. By incorporating $name$ into the molecular design of these ligands, chemists can achieve enhanced catalytic performance and efficiency in a range of chemical transformations.Overall, the application of Quinolin-3-ylmethanamine dihydrochloride in chemical synthesis encompasses a wide array of processes, showcasing its significance in advancing the field of organic chemistry and enabling the creation of diverse molecular structures with exceptional properties.