(S)-2-Amino-1,1,3-triphenyl-1-propanol

≥98%,≥99% e.e.

Reagent Code: #60137
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CAS Number 79868-78-3

science Other reagents with same CAS 79868-78-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.4 g/mol
Formula C₂₁H₂₁NO
thermostat Physical Properties
Melting Point 139-144°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral building block or ligand in catalytic reactions. Its unique structure, featuring three phenyl groups and a chiral center, makes it effective in inducing enantioselectivity in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, particularly in the production of chiral drugs where specific enantiomers are required for therapeutic efficacy. Additionally, it finds application in the development of advanced materials and as a resolving agent in the separation of racemic mixtures. Its steric and electronic properties make it a valuable tool in organic chemistry research and industrial processes.

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Test Parameter Specification
APPEARANCE White to Off-white Powder or Crystals
Purity (%) 97.5-100
e.e% 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿9,837.00

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(S)-2-Amino-1,1,3-triphenyl-1-propanol
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This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral building block or ligand in catalytic reactions. Its unique structure, featuring three phenyl groups and a chiral center, makes it effective in inducing enantioselectivity in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, particularly in the production of chiral drugs where specific enantiomers are required for therapeutic efficacy. Additionally, it finds appli
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral building block or ligand in catalytic reactions. Its unique structure, featuring three phenyl groups and a chiral center, makes it effective in inducing enantioselectivity in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, particularly in the production of chiral drugs where specific enantiomers are required for therapeutic efficacy. Additionally, it finds application in the development of advanced materials and as a resolving agent in the separation of racemic mixtures. Its steric and electronic properties make it a valuable tool in organic chemistry research and industrial processes.
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