3-Amino-5-methylpyridine, HCl


Chemical Name: 3-Amino-5-methylpyridine, HCl
CAS Number: 957065-90-6
Product Number: AG00H814(AGN-PC-0WA821)
Synonyms:
MDL No:
Molecular Formula: C6H9ClN2
Molecular Weight: 144.6021

Identification/Properties


Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
144.602g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
144.045g/mol
Monoisotopic Mass:
144.045g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
72.9
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:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-Methylpyridin-3-amine hydrochloride is a versatile chemical compound widely used in chemical synthesis processes. It serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique structure and reactivity, this compound plays a crucial role in the development of new compounds with diverse applications.In chemical synthesis, 5-Methylpyridin-3-amine hydrochloride can be employed as a key intermediate for the preparation of complex molecules. Its functional groups allow for selective modifications and reactions, leading to the formation of desired products with high efficiency and precision. Whether it is utilized for introducing specific substituents, forming bonds with other molecules, or initiating cascade reactions, this compound enables chemists to design and synthesize novel compounds with tailored properties.Furthermore, the use of 5-Methylpyridin-3-amine hydrochloride in chemical synthesis offers opportunities for the development of new drugs, pesticides, and other biologically active compounds. By incorporating this compound into synthetic routes, researchers can access structurally diverse molecules with potential therapeutic or agricultural benefits. Its versatility and compatibility with various synthetic methodologies make it a valuable tool in the realm of organic chemistry and drug discovery.