(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 |
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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 |
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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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