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58785-07-2

3-CHLORO-2-MORPHOLIN-4-YLANILINE

Catalog#: AR00EEO7  |   CAS#: 58785-07-2  |   MDL#: MFCD03821863  |   MF: C10H13ClN2O  |   MW: 212.676

Packsize Purity Price Availability Quantity
50mg 95% $52.00 2-3 weeks Buy Now Add To Cart
100mg 95% $61.00 2-3 weeks Buy Now Add To Cart
250mg 95% $76.00 2-3 weeks Buy Now Add To Cart
500mg 95% $105.00 2-3 weeks Buy Now Add To Cart
1g 95% $129.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $208.00 2-3 weeks Buy Now Add To Cart
5g 95% $342.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00EEO7
Chemical Name 3-CHLORO-2-MORPHOLIN-4-YLANILINE
CAS Number 58785-07-2
Molecular Formula C10H13ClN2O
Molecular Weight 212.676
MDL Number MFCD03821863
SMILES Nc1cccc(c1N1CCOCC1)Cl

3-Chloro-2-morpholinoaniline is a versatile chemical compound widely employed in organic synthesis processes. Its unique molecular structure, combining a chloro and a morpholino group on a central aniline ring, allows for a range of applications in chemical research and development.In chemical synthesis, 3-Chloro-2-morpholinoaniline serves as a valuable building block for the creation of complex molecules. Due to the presence of the chloro group, it can participate in nucleophilic substitution reactions to introduce the aniline backbone into various organic frameworks. The morpholino group, on the other hand, can act as a versatile protecting group, shielding reactive sites within a molecule during a synthetic sequence and selectively deprotecting under specific conditions, enabling precise control over chemical transformations.Furthermore, the presence of both electron-donating and electron-withdrawing groups in 3-Chloro-2-morpholinoaniline enhances its reactivity and compatibility with a variety of coupling reactions, such as Suzuki-Miyaura cross-coupling and Buchwald-Hartwig amination, facilitating the synthesis of biologically active compounds, pharmaceutical intermediates, and functional materials.Overall, the strategic incorporation of 3-Chloro-2-morpholinoaniline in chemical synthesis provides chemists with a powerful tool to construct diverse molecular architectures and advance the exploration of new chemical entities with potential applications in drug discovery, materials science, and beyond.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
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