tert-Butyl 4-amino-2-hydroxybenzoate
≥95%
- Product Code: 119005
CAS:
889858-34-8
| Molecular Weight: | 209.24 g./mol | Molecular Formula: | C₁₁H₁₅NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08703412 | |
| Melting Point: | Boiling Point: | 347.7±22.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both amino and hydroxyl groups, makes it a versatile building block in organic synthesis, enabling the creation of complex molecules with potential therapeutic applications. It is often employed in the preparation of compounds with anti-inflammatory, analgesic, or antimicrobial properties. Additionally, its ester group provides stability and reactivity, making it suitable for use in controlled-release drug formulations. In research settings, it serves as a precursor for studying structure-activity relationships in drug design, contributing to the development of novel medications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,967.00 |
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| 1.000 | 10-20 days | ฿11,916.00 |
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tert-Butyl 4-amino-2-hydroxybenzoate
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both amino and hydroxyl groups, makes it a versatile building block in organic synthesis, enabling the creation of complex molecules with potential therapeutic applications. It is often employed in the preparation of compounds with anti-inflammatory, analgesic, or antimicrobial properties. Additionally, its ester group provides stability and reactivity, making it suitable for use in controlled-release drug formulations. In research settings, it serves as a precursor for studying structure-activity relationships in drug design, contributing to the development of novel medications.
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