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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)-

7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride

Brc1ccc2c(c1)C(N)CCC2.Cl Request for Quotation
Chemical Name: 7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
CAS Number: 1199782-93-8
Product Number: AG000PYQ(AGN-PC-0WAMLN)
Synonyms:
MDL No: MFCD08544186
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:
0
Undefined Atom Stereocenter Count:
1
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride serves as a versatile building block for the creation of various organic compounds. This compound can be used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique molecular structure allows for selective functionalization reactions, enabling the introduction of specific functional groups at desired positions. Additionally, the presence of the bromine atom provides a site for further elaboration through cross-coupling reactions, making it a valuable tool for the synthesis of complex molecules.