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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)-

1-Naphthalenemethanamine,N-[[4-(1,1-dimethylethyl)phenyl]methyl]-N-methyl-, hydrochloride

CN(Cc1cccc2c1cccc2)Cc1ccc(cc1)C(C)(C)C.Cl Request for Quotation
Chemical Name: 1-Naphthalenemethanamine,N-[[4-(1,1-dimethylethyl)phenyl]methyl]-N-methyl-, hydrochloride
CAS Number: 101827-46-7
Product Number: AG0005NO(AGN-PC-0OQZTS)
Synonyms:
MDL No:
Molecular Formula: C23H28ClN
Molecular Weight: 353.9281

Identification/Properties

Properties
MP:
208-210°C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
353.934g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
5
Exact Mass:
353.191g/mol
Monoisotopic Mass:
353.191g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
374
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, N-(p-tert-Butylbenzyl)-N-methyl-1-naphthalenemethylamine hydrochloride is often used as a valuable reagent due to its ability to act as a versatile intermediate in various reactions. This compound serves as a key building block in the creation of complex organic molecules, making it a crucial component in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity allow for efficient and selective transformations, enabling chemists to streamline synthetic pathways and achieve high yields of desired products. Additionally, the presence of the tert-butylbenzyl and methyl groups provides steric and electronic effects that can influence the outcomes of chemical reactions, making this compound a valuable tool for chemists seeking to control the selectivity and efficiency of their synthetic processes.