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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)-

(S)-5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride

N[C@H]1CCCc2c1cccc2Br.Cl Request for Quotation
Chemical Name: (S)-5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
CAS Number: 1810074-82-8
Product Number: AG0022LJ(AGN-PC-0WAM9H)
Synonyms:
MDL No:
Molecular Formula: C10H13BrClN
Molecular Weight: 262.5739

Identification/Properties

Computed Properties
Molecular Weight:
262.575g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
260.992g/mol
Monoisotopic Mass:
260.992g/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


(S)-5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride is a valuable chemical compound widely used in chemical synthesis. This compound serves as a versatile building block in organic chemistry, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its chiral nature, owing to the (S)-configuration, makes it especially useful in asymmetric synthesis to access enantiomerically pure compounds.In chemical synthesis, (S)-5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride is often employed as a key intermediate in the construction of complex molecules with high stereochemical control. It can participate in various reactions such as reductive amination, nucleophilic substitution, and cyclization reactions to introduce the tetrahydronaphthalenylamine moiety into the target molecule. This compound's unique structural features and reactivity make it a valuable tool for organic chemists aiming to access biologically active compounds or functional materials with specific properties.Overall, the application of (S)-5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride in chemical synthesis enables the efficient and precise construction of diverse molecular scaffolds, showcasing its significance in the synthesis of complex organic molecules for various scientific and industrial applications.