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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)-

2-Naphthalenamine, 1,2,3,4-tetrahydro-5-methoxy-N-propyl-,hydrochloride, (R)-

CCCN[C@@H]1CCc2c(C1)cccc2OC.Cl Request for Quotation
Chemical Name: 2-Naphthalenamine, 1,2,3,4-tetrahydro-5-methoxy-N-propyl-,hydrochloride, (R)-
CAS Number: 93601-85-5
Product Number: AG00GTWI(AGN-PC-0W36KF)
Synonyms:
MDL No:
Molecular Formula: C14H22ClNO
Molecular Weight: 255.7836

Identification/Properties

Computed Properties
Molecular Weight:
255.786g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
255.139g/mol
Monoisotopic Mass:
255.139g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
207
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


The chemical compound (R)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine Hydrochloride is utilized in chemical synthesis for its role as a key intermediate in the production of various pharmaceutical compounds. This compound serves as a precursor in the synthesis of molecular structures with potential therapeutic applications. Through controlled chemical reactions and manipulations, (R)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine Hydrochloride can be transformed into more complex molecules with desired pharmacological properties. Its strategic placement in synthetic pathways allows for the efficient and targeted creation of novel drug candidates with potential benefits for medical treatment and research.