2-Pyridineethanamine, 6-methyl-


Chemical Name: 2-Pyridineethanamine, 6-methyl-
CAS Number: 19363-94-1
Product Number: AG003EYK(AGN-PC-0K6A22)
Synonyms:
MDL No:
Molecular Formula: C8H12N2
Molecular Weight: 136.1943

Identification/Properties


Properties
BP:
216.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
136.198g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
136.1g/mol
Monoisotopic Mass:
136.1g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
93.3
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



2-(6-Methylpyridin-2-yl)ethanamine, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound is primarily employed as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and functional groups make it a valuable intermediate for the synthesis of complex organic molecules.In chemical synthesis, 2-(6-Methylpyridin-2-yl)ethanamine serves as a crucial starting material for the preparation of diverse compounds with enhanced biological activities. Its incorporation into target molecules can modulate the properties and interactions of the resulting products, thereby influencing their efficacy and specificity. This compound is particularly valued for its ability to introduce specific structural features into organic frameworks, enabling the development of bioactive compounds with tailored properties.Furthermore, the reactivity of 2-(6-Methylpyridin-2-yl)ethanamine in various synthetic transformations allows for the efficient construction of molecular scaffolds with desired characteristics. By enabling the selective manipulation of functional groups and stereochemistry, this compound facilitates the synthesis of structurally complex molecules in a stepwise fashion. Its utility in chemical synthesis extends to the creation of novel compounds for medicinal research, agricultural applications, and material science.Overall, the strategic incorporation of 2-(6-Methylpyridin-2-yl)ethanamine in chemical synthesis offers researchers and chemists a versatile tool for the design and preparation of advanced organic compounds with diverse functionalities and applications.