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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)-

(R)-6-Chloro-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride

Clc1ccc2c(c1)CCC[C@H]2N.Cl Request for Quotation
Chemical Name: (R)-6-Chloro-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
CAS Number: 1810074-75-9
Product Number: AG0022LQ(AGN-PC-0WCXGE)
Synonyms:
MDL No:
Molecular Formula: C10H13Cl2N
Molecular Weight: 218.1229

Identification/Properties

Computed Properties
Molecular Weight:
218.121g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
217.043g/mol
Monoisotopic Mass:
217.043g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
160
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 (R)-6-Chloro-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride is an essential compound utilized in chemical synthesis for its versatile applications. In synthetic chemistry, this compound serves as a key intermediate in the construction of various pharmaceuticals, agrochemicals, and fine chemicals. Its chiral nature plays a crucial role in controlling the stereochemistry of the synthesized molecules, making it a valuable building block in asymmetric synthesis strategies. Additionally, the (R)-6-Chloro-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride can be employed as a catalyst or a ligand in catalytic processes, enabling selective transformations in organic reactions. Its unique molecular structure and reactivity make it a valuable tool for chemists working in drug discovery, materials science, and other research areas where precise control over stereochemistry and reactivity is required.