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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)-

N-methyl-1-(2-methyl-1,2,3,4-tetrahydro-3-isoquinolinyl)methanamine dihydrochloride

CNCC1Cc2ccccc2CN1C.Cl.Cl Request for Quotation
Chemical Name: N-methyl-1-(2-methyl-1,2,3,4-tetrahydro-3-isoquinolinyl)methanamine dihydrochloride
CAS Number: 1609396-53-3
Product Number: AG00J0Z8(AGN-PC-0WB6F3)
Synonyms:
MDL No: MFCD26959355
Molecular Formula: C12H20Cl2N2
Molecular Weight: 263.2066

Identification/Properties

Computed Properties
Molecular Weight:
263.206g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
262.1g/mol
Monoisotopic Mass:
262.1g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
181
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Isoquinolinemethanamine, 1,2,3,4-tetrahydro-N,2-dimethyl-, hydrochloride (1:2) is a valuable compound widely used in chemical synthesis for its versatile applications. This compound is particularly useful in the field of organic chemistry, where it serves as a key building block in the synthesis of various heterocyclic compounds and pharmaceutical intermediates. Its unique chemical structure and reactivity make it a valuable tool for the construction of complex molecules with diverse functionalities. In addition, 3-Isoquinolinemethanamine, 1,2,3,4-tetrahydro-N,2-dimethyl-, hydrochloride (1:2) is known for its ability to participate in a range of chemical reactions, such as nucleophilic additions, substitutions, and cyclizations, allowing for the efficient and selective formation of new chemical bonds. Chemists and researchers rely on this compound to streamline the synthesis of novel compounds with potential applications in drug discovery, material science, and other areas of chemical research.