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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, 5-chloro-2-methyl-

Cc1ncc(c(c1)N)Cl Request for Quotation
Chemical Name: 4-Pyridinamine, 5-chloro-2-methyl-
CAS Number: 97944-44-0
Product Number: AG003KQ1(AGN-PC-00MI1P)
Synonyms:
MDL No: MFCD07374907
Molecular Formula: C6H7ClN2
Molecular Weight: 142.5862

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
142.586g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
142.03g/mol
Monoisotopic Mass:
142.03g/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

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-Chloro-2-methyl-4-pyridinamine, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly used in the pharmaceutical industry for the development of various drugs and pharmaceutical intermediates due to its unique structure and reactivity.One of the key applications of 5-Chloro-2-methyl-4-pyridinamine is in the synthesis of heterocyclic compounds, which are essential building blocks in medicinal chemistry. By incorporating this compound into chemical reactions, chemists can efficiently construct complex molecular structures with specific biological activities. Its chlorine and methyl substituents provide opportunities for selective functionalization, enabling the synthesis of diverse chemical scaffolds.Moreover, 5-Chloro-2-methyl-4-pyridinamine can serve as a precursor for the introduction of functional groups such as amines, heterocycles, and halogens into organic molecules. This enables chemists to tailor the properties of the final compounds for specific purposes, including drug discovery, materials science, and agrochemical research.Overall, the strategic use of 5-Chloro-2-methyl-4-pyridinamine in chemical synthesis highlights its importance as a key building block for creating novel molecules with potential applications in various fields of science and technology.