(R)-(-)-4-Isopropyl-3-propionyl-2-oxazolidinone

98.0%

  • Product Code: 60202
  CAS:    89028-40-0
Molecular Weight: 185.22 g./mol Molecular Formula: C₉H₁₅NO₃
EC Number: MDL Number: MFCD00269691
Melting Point: Boiling Point:
Density: 1.10 Storage Condition: 2~8°C
Product Description: This chemical is primarily used as a chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically pure compounds. It is particularly valuable in the synthesis of pharmaceuticals, where it helps control stereochemistry during reactions like aldol additions, alkylations, and Diels-Alder reactions. Its rigid structure and ability to induce high enantioselectivity make it a preferred choice in the development of complex organic molecules, including active pharmaceutical ingredients (APIs) and fine chemicals. Additionally, it finds applications in academic research for studying stereoselective transformations and developing new synthetic methodologies.
Product Specification:
Test Specification
OPTICAL PURITY 98-100
PurityGC 98 100%
REFRACTIVE INDEX N20D 1.463-1.467
SPECIFIC GRAVITY 2020 1.093-1.101
SPECIFIC ROTATION A20DNEAT 87-92
APPEARANCE Colorless to yellow liquid
INFRARED SPECTROMETRY Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿860.00
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-
1.000 10-20 days ฿3,180.00
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(R)-(-)-4-Isopropyl-3-propionyl-2-oxazolidinone
This chemical is primarily used as a chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically pure compounds. It is particularly valuable in the synthesis of pharmaceuticals, where it helps control stereochemistry during reactions like aldol additions, alkylations, and Diels-Alder reactions. Its rigid structure and ability to induce high enantioselectivity make it a preferred choice in the development of complex organic molecules, including active pharmaceutical ingredients (APIs) and fine chemicals. Additionally, it finds applications in academic research for studying stereoselective transformations and developing new synthetic methodologies.
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