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CAS 58520-03-9

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(1S,2S)-1,2-bis(4-methoxy phenyl) ethane-1,2-diamine

Description:
(1S,2S)-1,2-bis(4-methoxy phenyl) ethane-1,2-diamine, with the CAS number 58520-03-9, is an organic compound characterized by its specific stereochemistry and functional groups. This compound features a central ethane backbone with two amine groups (-NH2) and two para-methoxyphenyl substituents, which contribute to its overall structure and properties. The presence of methoxy groups enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. The stereochemistry indicated by (1S,2S) suggests that the compound has specific spatial arrangements that can affect its biological activity and binding properties. Such compounds are often studied for their potential applications in pharmaceuticals, particularly in the development of drugs that target specific receptors or enzymes. Additionally, the presence of amine groups may allow for further derivatization, making it a versatile building block in organic synthesis. Overall, this compound's unique structure and functional groups make it of interest in both synthetic and medicinal chemistry.
Formula:C16H20N2O2
InChI:InChI=1/C16H20N2O2/c1-19-13-7-3-11(4-8-13)15(17)16(18)12-5-9-14(20-2)10-6-12/h3-10,15-16H,17-18H2,1-2H3/t15-,16-/m0/s1
SMILES:COc1ccc(cc1)[C@@H]([C@H](c1ccc(cc1)OC)N)N
Synonyms:
  • (1R,2R)-Bis(4-methoxyphenyl)-1,2-ethanediamine
  • 1S,2S-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethan
  • 1,2-Bis(4-Methoxyphenyl)Ethane-1,2-Diamine
  • (1R,2R)-1,2-bis(4-methoxyphenyl)ethane-1,2-diamine
  • (1S,2S)-1,2-bis(4-methoxyphenyl)ethane-1,2-diamine
  • (1S,2S)-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethane
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