(R)-2-Amino-2-(thiophen-2-yl)acetic acid
95%
- Product Code: 57091
CAS:
65058-23-3
| Molecular Weight: | 157.19 g./mol | Molecular Formula: | C₆H₇NO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00079612 | |
| Melting Point: | Boiling Point: | 311.8 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research, particularly in the development of chiral molecules. Its structure, featuring a thiophene ring and an amino acid moiety, makes it a valuable building block for synthesizing enantiomerically pure compounds. These compounds are often explored for their potential as active pharmaceutical ingredients (APIs) in drugs targeting neurological disorders, such as epilepsy or Parkinson's disease, due to their ability to interact with specific receptors in the brain. Additionally, it serves as a precursor in organic synthesis for creating complex molecules with potential therapeutic applications. Its chiral nature also makes it useful in asymmetric synthesis, where it aids in producing compounds with high stereochemical purity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,745.00 |
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| 0.250 | 10-20 days | ฿5,481.00 |
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| 1.000 | 10-20 days | ฿13,617.00 |
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(R)-2-Amino-2-(thiophen-2-yl)acetic acid
This compound is primarily utilized in the field of pharmaceutical research, particularly in the development of chiral molecules. Its structure, featuring a thiophene ring and an amino acid moiety, makes it a valuable building block for synthesizing enantiomerically pure compounds. These compounds are often explored for their potential as active pharmaceutical ingredients (APIs) in drugs targeting neurological disorders, such as epilepsy or Parkinson's disease, due to their ability to interact with specific receptors in the brain. Additionally, it serves as a precursor in organic synthesis for creating complex molecules with potential therapeutic applications. Its chiral nature also makes it useful in asymmetric synthesis, where it aids in producing compounds with high stereochemical purity.
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