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Catalog Number:
39498
CAS Number:
23190-16-1
(1R,2S)-(-)-2-Amino-1,2-diphenylethanol
Purity:
≥ 99% (Chiral HPLC, HPLC)
Documents
$18.53 /1G
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Product Information

(1R,2S)-(-)-2-Amino-1,2-diphenylethanol is a versatile chiral amine that plays a significant role in various chemical syntheses and applications. This compound is recognized for its ability to act as a building block in the production of pharmaceuticals, particularly in the synthesis of chiral intermediates and active pharmaceutical ingredients (APIs). Its unique stereochemistry allows for the development of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for ensuring the efficacy and safety of medications.

In addition to its pharmaceutical applications, (1R,2S)-(-)-2-Amino-1,2-diphenylethanol is also utilized in organic synthesis and catalysis, where it can serve as a ligand in asymmetric reactions. Researchers appreciate its effectiveness in promoting selectivity in reactions, making it a valuable asset in the development of new materials and fine chemicals. With its proven track record in enhancing reaction outcomes and its relevance in cutting-edge research, this compound is an essential choice for professionals seeking reliable and efficient solutions in their chemical processes.

CAS Number
23190-16-1
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C14H15NO
Molecular Weight
213.28
MDL Number
MFCD00074960
PubChem ID
22243
Melting Point
141 - 144 ?C
Appearance
White to pale yellow crystal or powder
Optical Rotation
[a]20D = -6 to -8 ° (C=0.6 in EtOH)
Conditions
Store at RT
General Information
CAS Number
23190-16-1
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C14H15NO
Molecular Weight
213.28
MDL Number
MFCD00074960
PubChem ID
22243
Melting Point
141 - 144 ?C
Appearance
White to pale yellow crystal or powder
Optical Rotation
[a]20D = -6 to -8 ° (C=0.6 in EtOH)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(1R,2S)-(-)-2-Amino-1,2-diphenylethanol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a chiral building block in the synthesis of various pharmaceuticals, particularly in creating drugs that require specific stereochemistry for optimal efficacy.
  • Catalysis: It is employed in asymmetric catalysis, aiding in the production of enantiomerically pure compounds, which is crucial in the manufacture of many fine chemicals and agrochemicals.
  • Biochemical Research: Researchers use it as a tool in studying enzyme mechanisms and interactions due to its ability to mimic natural substrates, providing insights into biological processes.
  • Material Science: This compound is explored for its potential in developing novel materials, including polymers and coatings, that require specific mechanical and thermal properties.
  • Analytical Chemistry: It is utilized in chiral chromatography, allowing for the separation and analysis of enantiomers in complex mixtures, which is essential for quality control in various industries.

Citations