1187930-70-6 | 2-Amino-2-pyridin-3-yl-ethanol dihydrochloride

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$163.00	$114.00
250mg	95%	in stock	$217.00	$152.00
500mg	95%	in stock	$361.00	$253.00
1g	95%	in stock	$541.00	$379.00

Description

• Catalog Number: AE22832
• Chemical Name: 2-Amino-2-pyridin-3-yl-ethanol dihydrochloride
• CAS Number: 1187930-70-6
• Molecular Formula: C7H12Cl2N2O
• Molecular Weight: 211.089
• MDL Number: MFCD12913796
• SMILES: OCC(c1cccnc1)N.Cl.Cl

Upstream Synthesis Route

2-Amino-2-(pyridin-3-yl)ethanol dihydrochloride is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its primary application lies in the synthesis of heterocyclic compounds and complex organic molecules, where it acts as a key intermediate in multi-step synthesis routes.In chemical synthesis, 2-Amino-2-(pyridin-3-yl)ethanol dihydrochloride plays a significant role as a nucleophilic reagent, enabling the introduction of the amino and pyridine functionalities into target molecules. This compound is particularly valued for its ability to participate in a wide range of reactions, including nucleophilic substitution, condensation, and cyclization reactions. By incorporating this compound into the synthetic pathway, chemists can access diverse chemical space and rapidly develop structurally intricate compounds with tailored properties.Moreover, the presence of the dihydrochloride salt in 2-Amino-2-(pyridin-3-yl)ethanol provides added versatility in organic synthesis, allowing for facile purification and isolation of the desired product. This salt form enhances the compound's solubility in common organic solvents, making it compatible with various reaction conditions and facilitating its integration into synthetic protocols.Overall, the use of 2-Amino-2-(pyridin-3-yl)ethanol dihydrochloride in chemical synthesis offers a strategic advantage to synthetic chemists by enabling the efficient construction of complex molecules with diverse functionality and structural motifs. Its versatile reactivity and compatibility with standard synthetic procedures make it a valuable tool for drug discovery, materials science, and agricultural chemistry applications.