(R)-3-Amino-4-(o-tolyl)butanoic acid
97%
- Product Code: 37618
CAS:
269398-79-0
| Molecular Weight: | 193.24 g./mol | Molecular Formula: | C₁₁H₁₅NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11870812 | |
| Melting Point: | Boiling Point: | 496.0±45.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
(R)-3-Amino-4-(o-tolyl)butanoic acid finds its primary application in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, such as epilepsy and Parkinson's disease, due to its structural similarity to gamma-aminobutyric acid (GABA), a crucial neurotransmitter. Additionally, this compound is utilized in the production of chiral molecules, where its stereochemistry plays a significant role in enhancing the efficacy and specificity of therapeutic agents. Its versatility also extends to research applications, where it serves as a building block for studying enzyme interactions and designing novel inhibitors for specific biochemical pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,925.00 |
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| 0.250 | 10-20 days | ฿5,850.00 |
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(R)-3-Amino-4-(o-tolyl)butanoic acid
(R)-3-Amino-4-(o-tolyl)butanoic acid finds its primary application in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, such as epilepsy and Parkinson's disease, due to its structural similarity to gamma-aminobutyric acid (GABA), a crucial neurotransmitter. Additionally, this compound is utilized in the production of chiral molecules, where its stereochemistry plays a significant role in enhancing the efficacy and specificity of therapeutic agents. Its versatility also extends to research applications, where it serves as a building block for studying enzyme interactions and designing novel inhibitors for specific biochemical pathways.
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