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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)-

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

NC1CCCc2c1cccc2Br.Cl Request for Quotation
Chemical Name: 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
CAS Number: 1810070-15-5
Product Number: AG0022L9(AGN-PC-0WAM9G)
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:
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


5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride is a valuable chemical compound that finds significant application in chemical synthesis processes. This compound serves as a crucial building block in the creation of various organic molecules due to its unique structural properties and reactivity.In chemical synthesis, 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride is commonly utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its versatile nature allows it to participate in a range of reactions, such as nucleophilic substitutions, condensations, and cyclizations, leading to the formation of complex molecular structures.Furthermore, the presence of both a bromine atom and an amine group in this compound enables chemists to introduce specific functional groups or stereochemical features into target molecules with precision. By incorporating 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride into synthetic pathways, chemists can access diverse chemical derivatives with tailored properties and functionalities.Overall, the strategic use of 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride in chemical synthesis plays a crucial role in advancing the development of novel compounds for various applications, showcasing its significance in modern organic chemistry practices.