2-Amino-2-(2-hydroxyphenyl)acetic acid
≥95%
- Product Code: 43719
CAS:
25178-38-5
Molecular Weight: | 167.16 g./mol | Molecular Formula: | C₈H₉NO₃ |
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EC Number: | MDL Number: | MFCD00014348 | |
Melting Point: | Boiling Point: | 358.8°C at 760 mmHg | |
Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical agents, particularly those targeting neurological and psychiatric disorders. It serves as a key intermediate in the production of drugs that modulate neurotransmitter systems, such as GABAergic and glutamatergic pathways. Additionally, it is employed in the development of chelating agents for metal ions, which can be applied in medical imaging and detoxification therapies. Its structural properties also make it a candidate for research in designing enzyme inhibitors and receptor modulators, contributing to advancements in medicinal chemistry.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White to Pale-yellow to Light-red to Brown Solid |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,390.00 |
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0.250 | 10-20 days | ฿5,650.00 |
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1.000 | 10-20 days | ฿18,880.00 |
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5.000 | 10-20 days | ฿86,990.00 |
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2-Amino-2-(2-hydroxyphenyl)acetic acid
This compound is primarily utilized in the synthesis of pharmaceutical agents, particularly those targeting neurological and psychiatric disorders. It serves as a key intermediate in the production of drugs that modulate neurotransmitter systems, such as GABAergic and glutamatergic pathways. Additionally, it is employed in the development of chelating agents for metal ions, which can be applied in medical imaging and detoxification therapies. Its structural properties also make it a candidate for research in designing enzyme inhibitors and receptor modulators, contributing to advancements in medicinal chemistry.
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