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N-[(1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide

  • CAS No. 887924-07-4

  • Cat. No. CS-0133261
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

N-[(1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide|CS-0133261

Structure of 887924-07-4

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General Information

  • CAS No. 887924-07-4
  • Cat. No. CS-0133261
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, stored under nitrogen, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₃H₂₆N₂O₄S
  • Molecular Weight 426.53
  • Synonym(s) N-[(1S,2S)-2-aMino-1,2-bis(4-Methoxyphenyl)ethyl]-4-Methyl-BenzenesulfonaMide
  • SMILES O=S(C1=CC=C(C)C=C1)(N[C@@H](C2=CC=C(OC)C=C2)[C@@H](N)C3=CC=C(OC)C=C3)=O

Description

N-[(1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide features a chiral diamine scaffold flanked by two methoxy-substituted phenyl groups, enabling precise stereocontrolled synthesis. The sulfonamide moiety delivers enhanced solubility and hydrogen-bonding capacity, facilitating integration into bioactive molecule architectures under standard conditions.

Application

N-[(1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide serves as a chiral auxiliary in asymmetric synthesis, leveraging its rigid binaphthyl-like scaffold and amine functionality to direct stereoselective transformations. The sulfonamide group enhances solubility and facilitates purification, while the methoxy-substituted aryl moieties contribute to stability and compatibility with standard coupling reactions. This compound functions effectively in enantioselective derivatization and transition-metal-catalyzed processes.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   90.65
  • LogP   3.73182
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   8

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