(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 |
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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 |
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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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