(R)-()-Tetrahydro-3-furylamine p-toluenesulfonate

98%

  • Product Code: 73145
  CAS:    111769-27-8
Molecular Weight: 259.32 g./mol Molecular Formula: C₄H₉NOC₇H₈O₃S
EC Number: MDL Number: MFCD00040622
Melting Point: 139-141°C Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: (R)-()-Tetrahydro-3-furylamine p-toluenesulfonate is primarily used in the field of organic synthesis as a chiral building block. Its application is significant in the production of pharmaceuticals, where it serves as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). The compound's chiral nature makes it valuable in the development of enantiomerically pure drugs, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in the preparation of complex molecules for research purposes, aiding in the study of stereochemistry and reaction mechanisms. Its role in asymmetric synthesis is particularly noteworthy, as it helps in creating compounds with high optical purity, which is essential for many therapeutic agents.
Product Specification:
Test Specification
APPEARANCE White to light yellow Solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿2,120.00
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5.000 10-20 days ฿7,750.00
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(R)-()-Tetrahydro-3-furylamine p-toluenesulfonate
(R)-()-Tetrahydro-3-furylamine p-toluenesulfonate is primarily used in the field of organic synthesis as a chiral building block. Its application is significant in the production of pharmaceuticals, where it serves as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). The compound's chiral nature makes it valuable in the development of enantiomerically pure drugs, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in the preparation of complex molecules for research purposes, aiding in the study of stereochemistry and reaction mechanisms. Its role in asymmetric synthesis is particularly noteworthy, as it helps in creating compounds with high optical purity, which is essential for many therapeutic agents.
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