(S)-()-1-Phenyl-1,2-ethanediol 2-tosylate

98%

  • Product Code: 60218
  Alias:    (S)-(+)-1-Phenyl-1,2-ethylene glycol p-toluenesulfonate
  CAS:    40435-14-1
Molecular Weight: 292.35 g./mol Molecular Formula: CH₃C₆H₄SO₃CH₂CHC₆H₅OH
EC Number: MDL Number: MFCD00013428
Melting Point: 74-76 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: (S)-()-1-Phenyl-1,2-ethanediol 2-tosylate is primarily used as a chiral intermediate in organic synthesis. It plays a significant role in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals. This compound is often employed in asymmetric synthesis to create complex molecules with high stereochemical control. It is particularly valuable in the synthesis of chiral alcohols, amines, and other functional groups that are essential in active pharmaceutical ingredients (APIs). Additionally, it is utilized in the preparation of ligands for asymmetric catalysis, enhancing the efficiency and selectivity of catalytic reactions in drug discovery and development.
Product Specification:
Test Specification
CARBON 60 63.2%
Melting point 74 76?
NITROGENN 10.6 11.2%
OPTICAL ROTATION A20D2CH3CH2OH 31-37
PURITYHPLC 98 100%
APPEARANCE WHITE POWDER OR CRYSTALS
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿930.00
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(S)-()-1-Phenyl-1,2-ethanediol 2-tosylate
(S)-()-1-Phenyl-1,2-ethanediol 2-tosylate is primarily used as a chiral intermediate in organic synthesis. It plays a significant role in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals. This compound is often employed in asymmetric synthesis to create complex molecules with high stereochemical control. It is particularly valuable in the synthesis of chiral alcohols, amines, and other functional groups that are essential in active pharmaceutical ingredients (APIs). Additionally, it is utilized in the preparation of ligands for asymmetric catalysis, enhancing the efficiency and selectivity of catalytic reactions in drug discovery and development.
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