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Catalog Number:
30701
CAS Number:
29841-69-8
1 S ,2 S -(-)-1,2-Diphényléthylènediamine
Purity:
≥ 99,5 % (HPLC, pureté chirale)
Synonym(s):
(1 S ,2 S -(-)-1,2-diamino-1,2-diphényléthane
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Product Information

(1S,2S)-(-)-1,2-Diphenylethylenediamine is a versatile chiral diamine that plays a crucial role in various chemical synthesis processes. This compound is widely recognized for its application in asymmetric synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique chiral properties enable the creation of enantiomerically pure compounds, which are essential in the development of effective drugs with minimal side effects. Researchers and industry professionals appreciate its ability to facilitate reactions that yield high selectivity, making it a valuable tool in the synthesis of complex organic molecules.

In addition to its role in asymmetric synthesis, (1S,2S)-(-)-1,2-Diphenylethylenediamine is also utilized as a ligand in coordination chemistry, enhancing the efficiency of catalytic processes. Its compatibility with various metal ions allows for the development of highly effective catalysts that can be employed in fine chemical production. The compound's stability and ease of handling further contribute to its appeal in both laboratory and industrial settings, making it an indispensable resource for chemists aiming to innovate and optimize their synthetic pathways.

Synonyms
(1 S ,2 S -(-)-1,2-diamino-1,2-diphényléthane
CAS Number
29841-69-8
Purity
≥ 99,5 % (HPLC, pureté chirale)
Molecular Formula
C14H16N2
Molecular Weight
212.29
MDL Number
MFCD00082751
PubChem ID
110695
Melting Point
81-83 ?C
Appearance
Poudre cristalline blanche à jaune clair
Optical Rotation
[a] D 20 = -102 ± 1º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
(1 S ,2 S -(-)-1,2-diamino-1,2-diphényléthane
CAS Number
29841-69-8
Purity
≥ 99,5 % (HPLC, pureté chirale)
Molecular Formula
C14H16N2
Molecular Weight
212.29
MDL Number
MFCD00082751
PubChem ID
110695
Melting Point
81-83 ?C
Appearance
Poudre cristalline blanche à jaune clair
Optical Rotation
[a] D 20 = -102 ± 1º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(1S,2S)-(-)-1,2-Diphenylethylenediamine is widely utilized in research focused on:

  • Chiral Catalysis: This compound serves as an effective chiral ligand in asymmetric synthesis, helping chemists produce enantiomerically pure compounds, which is crucial in pharmaceuticals.
  • Pharmaceutical Development: It plays a significant role in the development of new drugs, particularly in the synthesis of complex organic molecules that require precise stereochemistry.
  • Material Science: Used in the formulation of advanced materials, it enhances the properties of polymers and resins, improving their performance in various applications.
  • Analytical Chemistry: The compound is employed as a reagent in various analytical techniques, aiding in the detection and quantification of different substances in complex mixtures.
  • Biochemistry: It is utilized in biological studies to investigate enzyme mechanisms and interactions, providing insights into metabolic pathways and potential therapeutic targets.

Citations