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Catalog Number:
30717
CAS Number:
167316-27-0
1S,2S-(+)-N-p-Tosyl-1,2-diphenylethylenediamine
Purity:
≥ 99% (Assay, Chiral purity)
Documents
$51.18 /1G
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Product Information

(1S,2S)-(+)-N-p-Tosyl-1,2-diphenylethylenediamine is a versatile compound widely utilized in asymmetric synthesis and catalysis. This chiral diamine serves as an essential ligand in various catalytic reactions, particularly in the formation of chiral amines and other valuable intermediates. Its unique structure, featuring a tosyl group, enhances its reactivity and selectivity, making it a preferred choice for researchers aiming to develop enantiomerically pure compounds.

In the pharmaceutical industry, this compound plays a crucial role in the synthesis of biologically active molecules, contributing to the development of new drugs and therapeutic agents. Its ability to facilitate enantioselective transformations allows chemists to create compounds with specific desired properties, thereby streamlining the drug discovery process. Additionally, (1S,2S)-(+)-N-p-Tosyl-1,2-diphenylethylenediamine is recognized for its stability and ease of handling, making it an ideal candidate for both academic research and industrial applications.

CAS Number
167316-27-0
Purity
≥ 99% (Assay, Chiral purity)
Molecular Formula
C21H22N2O2S
Molecular Weight
366.48
MDL Number
MFCD03095684
PubChem ID
3608242
Melting Point
124-129 °C
Appearance
White to pale yellow crystalline powder
Optical Rotation
[a]D20 = +33° to +36º (C=1 in CHCl3)
Conditions
Store at 0-8 °C
General Information
CAS Number
167316-27-0
Purity
≥ 99% (Assay, Chiral purity)
Molecular Formula
C21H22N2O2S
Molecular Weight
366.48
MDL Number
MFCD03095684
PubChem ID
3608242
Melting Point
124-129 °C
Appearance
White to pale yellow crystalline powder
Optical Rotation
[a]D20 = +33° to +36º (C=1 in CHCl3)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(1S,2S)-(+)-N-p-Tosyl-1,2-diphenylethylenediamine is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a chiral auxiliary in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds efficiently, which is crucial in pharmaceuticals.
  • Catalysis: It is employed in catalytic processes, particularly in the synthesis of complex organic molecules, enhancing reaction selectivity and yield compared to traditional catalysts.
  • Drug Development: Researchers use this compound in the development of new drugs, especially in creating compounds that target specific biological pathways, improving therapeutic efficacy.
  • Material Science: It finds applications in the development of advanced materials, such as polymers and nanomaterials, due to its unique structural properties that enhance material performance.
  • Analytical Chemistry: This chemical is utilized in various analytical techniques, including chromatography and spectroscopy, to improve the separation and identification of complex mixtures.

Citations