2-Amino-2-(tetrahydro-2H-pyran-4-yl)acetic acid
95%
- Product Code: 45732
CAS:
53284-84-7
| Molecular Weight: | 159.18 g./mol | Molecular Formula: | C₇H₁₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02183576 | |
| Melting Point: | Boiling Point: | 316.7°C at 760 mmHg | |
| Density: | 1.211g/cm3 | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and metabolic disorders. Its structure, featuring both an amino group and a tetrahydro-2H-pyran ring, makes it a versatile building block for creating compounds with potential therapeutic properties. Additionally, it is explored in the design of peptidomimetics and small-molecule inhibitors, which are crucial in drug discovery efforts aimed at treating diseases such as cancer, diabetes, and neurodegenerative conditions. Its unique chemical framework also allows for modifications to enhance drug-like properties, including solubility and bioavailability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $36.25 |
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| 1.000 | 10-20 days | $88.21 |
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| 5.000 | 10-20 days | $387.22 |
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2-Amino-2-(tetrahydro-2H-pyran-4-yl)acetic acid
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and metabolic disorders. Its structure, featuring both an amino group and a tetrahydro-2H-pyran ring, makes it a versatile building block for creating compounds with potential therapeutic properties. Additionally, it is explored in the design of peptidomimetics and small-molecule inhibitors, which are crucial in drug discovery efforts aimed at treating diseases such as cancer, diabetes, and neurodegenerative conditions. Its unique chemical framework also allows for modifications to enhance drug-like properties, including solubility and bioavailability.
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