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Catalog Number:
30700
CAS Number:
35132-20-8
1 R ,2 R -(+)-1,2-Diphényléthylènediamine
Purity:
≥ 99,5 % (HPLC, pureté chirale)
Synonym(s):
(1 R ,2 R -(+)-1,2-Diamino-1,2-diphényléthane
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Product Information

(1R,2R)-(+)-1,2-Diphenylethylenediamine is a versatile compound widely utilized in various fields, particularly in organic synthesis and pharmaceutical research. This chiral diamine serves as a crucial building block in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. Its unique stereochemistry allows for the development of enantiomerically pure compounds, which is essential in the production of effective and safe drugs. Researchers appreciate its role as a ligand in asymmetric catalysis, where it enhances reaction selectivity and efficiency, making it invaluable in the development of new synthetic methodologies.

In addition to its synthetic applications, (1R,2R)-(+)-1,2-Diphenylethylenediamine is also employed in the preparation of various functional materials and polymers. Its ability to form stable complexes with metal ions opens avenues for its use in coordination chemistry and materials science. With its proven track record in enhancing reaction outcomes and its adaptability in diverse applications, this compound stands out as a preferred choice for professionals seeking reliable and effective solutions in their research and development endeavors.

Synonyms
(1 R ,2 R -(+)-1,2-Diamino-1,2-diphényléthane
CAS Number
35132-20-8
Purity
≥ 99,5 % (HPLC, pureté chirale)
Molecular Formula
C14H16N2
Molecular Weight
212.29
MDL Number
MFCD00082769
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 R ,2 R -(+)-1,2-Diamino-1,2-diphényléthane
CAS Number
35132-20-8
Purity
≥ 99,5 % (HPLC, pureté chirale)
Molecular Formula
C14H16N2
Molecular Weight
212.29
MDL Number
MFCD00082769
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

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

  • Chiral Catalysis: This compound serves as a chiral ligand in asymmetric synthesis, enhancing the production of enantiomerically pure compounds, which is crucial in pharmaceuticals.
  • Pharmaceutical Development: Its ability to form stable complexes with metal ions makes it valuable in drug formulation, particularly in creating more effective and targeted therapies.
  • Organic Synthesis: It is employed in various organic reactions, including the synthesis of complex molecules, thereby streamlining processes in chemical manufacturing.
  • Analytical Chemistry: The compound is used in chromatography as a chiral stationary phase, improving the separation and analysis of racemic mixtures in quality control labs.
  • Material Science: Its properties are harnessed in the development of advanced materials, particularly in creating polymers with enhanced thermal and mechanical properties.

Citations