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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)-

N-benzyl-4-bromopyridin-2-amine

Brc1ccnc(c1)NCc1ccccc1 Request for Quotation
Chemical Name: N-benzyl-4-bromopyridin-2-amine
CAS Number: 1209457-90-8
Product Number: AG00949S(AGN-PC-09PZRU)
Synonyms:
MDL No:
Molecular Formula: C12H11BrN2
Molecular Weight: 263.1331

Identification/Properties

Computed Properties
Molecular Weight:
263.138g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
262.011g/mol
Monoisotopic Mass:
262.011g/mol
Topological Polar Surface Area:
24.9A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
181
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Benzyl-4-bromopyridin-2-amine is a versatile compound widely used in chemical synthesis as a key building block. In organic chemistry, it serves as a valuable intermediate for the synthesis of various biologically active molecules, pharmaceuticals, and agrochemicals. With its unique chemical properties, N-Benzyl-4-bromopyridin-2-amine facilitates the introduction of functional groups and modifications to create novel compounds for research and industrial applications. Its strategic placement of the bromine and amino groups allows for selective reactions and efficient synthesis processes, making it a valuable tool for chemists in the development of new chemical entities.