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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)-

1-Naphthalenamine, 2,4-dibromo-

Brc1cc(Br)c2c(c1N)cccc2 Request for Quotation
Chemical Name: 1-Naphthalenamine, 2,4-dibromo-
CAS Number: 20191-76-8
Product Number: AG00BJQY(AGN-PC-0JP8LZ)
Synonyms:
MDL No: MFCD00155345
Molecular Formula: C10H7Br2N
Molecular Weight: 300.9773

Identification/Properties

Computed Properties
Molecular Weight:
300.981g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
300.892g/mol
Monoisotopic Mass:
298.895g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
186
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dibromonaphthalen-1-amine serves as a versatile building block in chemical synthesis due to its unique reactivity and structural properties. This compound is commonly utilized in the synthesis of various organic molecules and pharmaceuticals, particularly those requiring a nitrogen-containing aromatic scaffold. Its brominated naphthalene core provides opportunities for selective functionalization, enabling the introduction of diverse functional groups with high regioselectivity. In addition, the amino group offers a crucial site for further derivatization through various coupling reactions, such as amide formation, Suzuki coupling, or aromatic substitution. Overall, 2,4-Dibromonaphthalen-1-amine is a valuable intermediate for designing and accessing novel compounds with tailored properties for advanced chemical and pharmaceutical applications.