(S)-2-Amino-4-cyclohexylbutanoic acid
97%
- Product Code: 38301
CAS:
116622-38-9
Molecular Weight: | 185.26 g./mol | Molecular Formula: | C₁₀H₁₉NO₂ |
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EC Number: | MDL Number: | MFCD18252744 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, away 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 bioactive molecules, particularly those targeting neurological disorders. Its structure is often incorporated into peptides and small molecules designed to modulate specific receptors or enzymes in the brain, making it valuable for studying conditions like epilepsy, anxiety, and neurodegenerative diseases. Additionally, it is explored in the development of prodrugs, where its properties enhance the bioavailability and stability of therapeutic agents. Its chiral nature also makes it a useful building block in asymmetric synthesis for creating enantiomerically pure compounds.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | €33.00 |
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1.000 | 10-20 days | €82.15 |
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5.000 | 10-20 days | €248.84 |
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10.000 | 10-20 days | €415.75 |
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(S)-2-Amino-4-cyclohexylbutanoic 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 bioactive molecules, particularly those targeting neurological disorders. Its structure is often incorporated into peptides and small molecules designed to modulate specific receptors or enzymes in the brain, making it valuable for studying conditions like epilepsy, anxiety, and neurodegenerative diseases. Additionally, it is explored in the development of prodrugs, where its properties enhance the bioavailability and stability of therapeutic agents. Its chiral nature also makes it a useful building block in asymmetric synthesis for creating enantiomerically pure compounds.
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