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4930-99-8

(3-METHYL-PYRIDIN-2-YL)-HYDRAZINE

Catalog#: AR00DDOY  |   CAS#: 4930-99-8  |   MDL#: MFCD07786312  |   MF: C6H9N3  |   MW: 123.1558

Packsize Purity Price Availability Quantity
100mg 98% $9.00 Global Stock Buy Now Add To Cart
250mg 98% $14.00 Global Stock Buy Now Add To Cart
1g 98% $46.00 Global Stock Buy Now Add To Cart
5g 98% $229.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DDOY
Chemical Name (3-METHYL-PYRIDIN-2-YL)-HYDRAZINE
CAS Number 4930-99-8
Molecular Formula C6H9N3
Molecular Weight 123.1558
MDL Number MFCD07786312
SMILES NNc1ncccc1C
NSC Number 70718

2-Hydrazinyl-3-methylpyridine, also known as HMP, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. One of its key applications is as a building block in the synthesis of various heterocyclic compounds. By utilizing the hydrazine and pyridine moieties in its structure, 2-Hydrazinyl-3-methylpyridine can participate in a variety of organic reactions to form new complex molecules.In organic synthesis, 2-Hydrazinyl-3-methylpyridine can act as a nucleophile, reacting with various electrophiles to form stable adducts. This reactivity makes it a valuable reagent for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, the hydrazine functional group in 2-Hydrazinyl-3-methylpyridine enables it to undergo various transformations, such as oxidation, reduction, and condensation reactions, further expanding its synthetic utility.Moreover, the presence of the pyridine ring in 2-Hydrazinyl-3-methylpyridine imparts aromaticity and electron-donating properties, making it suitable for use in palladium-catalyzed cross-coupling reactions and other transition metal-catalyzed transformations. This reactivity can be harnessed to construct complex organic frameworks with precise control over regioselectivity and stereoselectivity.Overall, 2-Hydrazinyl-3-methylpyridine is a valuable tool in the toolbox of synthetic chemists, offering diverse opportunities for the construction of structurally complex and biologically relevant molecules through efficient and selective chemical transformations.
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