TERT-BUTYL (R)-1-(N-METHOXY-N-METHYLCARBAMOYL)-2-HYDROXYETHYLCARBAMATE
97%
- Product Code: 51169
CAS:
167102-61-6
Molecular Weight: | 248.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₅ |
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EC Number: | MDL Number: | ||
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Density: | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of chiral intermediates. It serves as a key building block in the production of enantiomerically pure pharmaceuticals, enabling the creation of drugs with high specificity and reduced side effects. Its structure is often exploited in peptide synthesis, where it acts as a protecting group for amino acids, ensuring selective reactions during complex molecular constructions. Additionally, it finds application in the synthesis of biologically active molecules, such as enzyme inhibitors and receptor modulators, which are critical in drug discovery and development. Its role in facilitating asymmetric synthesis makes it valuable for producing compounds with precise stereochemistry, essential for the efficacy of many therapeutic agents.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿11,835.00 |
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1.000 | 10-20 days | ฿24,561.00 |
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5.000 | 10-20 days | ฿74,061.00 |
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TERT-BUTYL (R)-1-(N-METHOXY-N-METHYLCARBAMOYL)-2-HYDROXYETHYLCARBAMATE
This compound is primarily utilized in the field of organic synthesis, particularly in the development of chiral intermediates. It serves as a key building block in the production of enantiomerically pure pharmaceuticals, enabling the creation of drugs with high specificity and reduced side effects. Its structure is often exploited in peptide synthesis, where it acts as a protecting group for amino acids, ensuring selective reactions during complex molecular constructions. Additionally, it finds application in the synthesis of biologically active molecules, such as enzyme inhibitors and receptor modulators, which are critical in drug discovery and development. Its role in facilitating asymmetric synthesis makes it valuable for producing compounds with precise stereochemistry, essential for the efficacy of many therapeutic agents.
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