()-4,5-Bis[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolane

97.0%

  • Product Code: 70768
  Alias:    (+)-2,3-O-isopropylidene-1,1,4,4-tetraphenyl-D-threitol (+)-trans-α,α′-(2,2-di Methyl-1,3-dioxolane-4,5-diyl)bis(diphenylmethanol)(4S,5S)-4,5-bis(diphenylhydroxymethyl)-2,2- Dimethyldioxolane(4S,5S)-2,2-dimethyl--1,3-dioxolane-4,5-diyl)bis(diphenylmethanol)​​
  CAS:    93379-49-8
Molecular Weight: 466.58 g./mol Molecular Formula: C₃₁H₃₀O₄
EC Number: MDL Number: MFCD00010079
Melting Point: 193-196 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily utilized as a chiral auxiliary or resolving agent in asymmetric synthesis. It aids in the formation of enantiomerically pure compounds, which is crucial in the production of pharmaceuticals and fine chemicals. Its structure allows it to effectively induce chirality in reactions, making it valuable in the synthesis of complex molecules with specific stereochemical requirements. Additionally, it can be employed in the development of chiral catalysts or ligands, enhancing the efficiency and selectivity of catalytic processes. Its application extends to research in organic chemistry, where it is used to study stereoselective reactions and develop new synthetic methodologies.
Product Specification:
Test Specification
Melting point 194-198
PURITYHPLC 97-100
SPECIFIC ROTATION A20DC1 CHCL3 62-71
APPEARANCE WHITE POWDER OR CRYSTALS
INFRARED SPECTROMETRY Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿290.00
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-
0.250 10-20 days ฿390.00
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1.000 10-20 days ฿580.00
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-
5.000 10-20 days ฿1,860.00
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-
25.000 10-20 days ฿8,140.00
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()-4,5-Bis[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolane
This chemical is primarily utilized as a chiral auxiliary or resolving agent in asymmetric synthesis. It aids in the formation of enantiomerically pure compounds, which is crucial in the production of pharmaceuticals and fine chemicals. Its structure allows it to effectively induce chirality in reactions, making it valuable in the synthesis of complex molecules with specific stereochemical requirements. Additionally, it can be employed in the development of chiral catalysts or ligands, enhancing the efficiency and selectivity of catalytic processes. Its application extends to research in organic chemistry, where it is used to study stereoselective reactions and develop new synthetic methodologies.
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