(R)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate

97%

  • Product Code: 87163
  CAS:    219823-47-9
Molecular Weight: 242.29 g./mol Molecular Formula: C₁₁H₁₄O₄S
EC Number: MDL Number: MFCD27947543
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, dry, sealed
Product Description: This chemical is primarily utilized in organic synthesis as a chiral building block. It is often employed in the preparation of pharmaceuticals and fine chemicals, where its stereochemistry plays a crucial role in the development of enantiomerically pure compounds. The compound is particularly valuable in asymmetric synthesis, enabling the creation of complex molecules with high optical purity. Additionally, it serves as an intermediate in the production of active pharmaceutical ingredients (APIs) and other biologically active compounds. Its sulfonate group makes it a useful precursor for further functionalization, allowing chemists to introduce various substituents in targeted synthetic pathways.
Product Specification:
Test Specification
APPEARANCE White to Off-white to Yellow to Red-brown Solid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
NOTE: This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid)
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿612.00
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-
0.250 10-20 days ฿1,251.00
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-
1.000 10-20 days ฿3,132.00
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-
(R)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate
This chemical is primarily utilized in organic synthesis as a chiral building block. It is often employed in the preparation of pharmaceuticals and fine chemicals, where its stereochemistry plays a crucial role in the development of enantiomerically pure compounds. The compound is particularly valuable in asymmetric synthesis, enabling the creation of complex molecules with high optical purity. Additionally, it serves as an intermediate in the production of active pharmaceutical ingredients (APIs) and other biologically active compounds. Its sulfonate group makes it a useful precursor for further functionalization, allowing chemists to introduce various substituents in targeted synthetic pathways.
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