(R)-()-α,α-Diphenylprolinol

99%

  • Product Code: 65704
  Alias:    α,α-Diphenyl-D-prolinol (R)-2-(diphenylhydroxymethyl)pyrrolidine +)-α,α-Diphenylprolinol (R)-(+)-α-Diphenyl-2-pyrrolidinemethanol
  CAS:    22348-32-9
Molecular Weight: 253.34 g./mol Molecular Formula: C₁₇H₁₉NO
EC Number: MDL Number: MFCD00077754
Melting Point: 77-80 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: Used as a chiral auxiliary in asymmetric synthesis, particularly in the formation of enantiomerically pure compounds. It is widely employed in organic chemistry to induce chirality in reactions such as aldol condensations, Michael additions, and Diels-Alder reactions. Its sterically demanding structure helps control the stereochemistry of the products, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, it serves as a precursor for chiral catalysts and ligands in transition metal-catalyzed processes, enhancing selectivity and efficiency in complex molecular transformations.
Product Specification:
Test Specification
Melting point 77 80?
PURITY TITRATION BY HCL04 98.5 101.5%
Purity 99 100%
Chloroform 65-69
APPEARANCE WHITE TO OFF-WHITE POWDER OR CRYSTALS
INFRARED SPECTRUM Conforms to Structure
SOLUBILITY IN CHLOROFORM almost transparency
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿300.00
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-
1.000 10-20 days ฿480.00
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5.000 10-20 days ฿800.00
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-
25.000 10-20 days ฿3,280.00
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-
100.000 10-20 days ฿10,680.00
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(R)-()-α,α-Diphenylprolinol
Used as a chiral auxiliary in asymmetric synthesis, particularly in the formation of enantiomerically pure compounds. It is widely employed in organic chemistry to induce chirality in reactions such as aldol condensations, Michael additions, and Diels-Alder reactions. Its sterically demanding structure helps control the stereochemistry of the products, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, it serves as a precursor for chiral catalysts and ligands in transition metal-catalyzed processes, enhancing selectivity and efficiency in complex molecular transformations.
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