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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-Naphthaleneethanamine, hydrochloride

NCCc1cccc2c1cccc2.Cl Request for Quotation
Chemical Name: 1-Naphthaleneethanamine, hydrochloride
CAS Number: 942-05-2
Product Number: AG003EPM(AGN-PC-0NISI7)
Synonyms:
MDL No:
Molecular Formula: C12H14ClN
Molecular Weight: 207.6993

Identification/Properties

Computed Properties
Molecular Weight:
207.701g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
207.081g/mol
Monoisotopic Mass:
207.081g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
155
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-(1-Naphthyl)ethylamine hydrochloride, when utilized in chemical synthesis, serves as a versatile building block in the creation of various organic compounds. This compound is particularly valuable in the preparation of pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it suitable for introducing the 2-(1-Naphthyl)ethylamine moiety into target molecules, enabling the modification of their properties or enhancing their biological activities. By incorporating 2-(1-Naphthyl)ethylamine hydrochloride into synthetic routes, chemists can access a wide range of structurally diverse and potentially valuable compounds for industrial and research applications.