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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)-

4-Pyridinamine, 3-bromo-5-methyl-

Nc1c(C)cncc1Br Request for Quotation
Chemical Name: 4-Pyridinamine, 3-bromo-5-methyl-
CAS Number: 97944-43-9
Product Number: AG0036RZ(AGN-PC-00MI1O)
Synonyms:
MDL No:
Molecular Formula: C6H7BrN2
Molecular Weight: 187.0372

Identification/Properties

Properties
BP:
290°C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
187.04g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
185.979g/mol
Monoisotopic Mass:
185.979g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
97.1
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


3-Bromo-5-methylpyridin-4-amine is a versatile chemical compound commonly used in organic synthesis for its unique properties and reactivity. One of the key applications of this compound is as a building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its specific structure, 3-Bromo-5-methylpyridin-4-amine serves as a valuable intermediate in the synthesis of biologically active molecules. Its bromine substituent allows for further functionalization through various reactions such as coupling, substitution, and cyclization, enabling the creation of complex molecular structures. Additionally, the presence of an amino group in the molecule provides opportunities for further derivatization, making it an essential component in the development of new compounds with desired properties. Researchers and chemists often utilize 3-Bromo-5-methylpyridin-4-amine in their synthetic endeavors to access novel compounds for medicinal, agricultural, and industrial applications.