4-Amino-4-(p-tolyl)butanoic acid hydrochloride
≥95%
- Product Code: 46982
CAS:
1810070-01-9
| Molecular Weight: | 229.70 g./mol | Molecular Formula: | C₁₁H₁₆ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28986164 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both an amino group and a carboxylic acid group, makes it a versatile building block for creating more complex molecules. Specifically, it is often employed in the development of drugs targeting the central nervous system, as well as in the synthesis of compounds with potential anti-inflammatory or analgesic properties. Additionally, it can be used in research settings to study biochemical pathways or to develop new therapeutic agents. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous environments during chemical reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,992.00 |
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| 0.250 | 10-20 days | ฿15,975.00 |
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4-Amino-4-(p-tolyl)butanoic acid hydrochloride
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both an amino group and a carboxylic acid group, makes it a versatile building block for creating more complex molecules. Specifically, it is often employed in the development of drugs targeting the central nervous system, as well as in the synthesis of compounds with potential anti-inflammatory or analgesic properties. Additionally, it can be used in research settings to study biochemical pathways or to develop new therapeutic agents. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous environments during chemical reactions.
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