2-((tert-Butoxycarbonyl)amino)-4-chlorobenzoic acid
97%
- Product Code: 145505
CAS:
136290-47-6
| Molecular Weight: | 271.7 g./mol | Molecular Formula: | C₁₂H₁₄ClNO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 352.4°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino groups are required. The Boc-protected amine allows for controlled deprotection during multi-step syntheses, enabling selective reactions without interference. The carboxylic acid functionality provides a site for amide bond formation, making it valuable in constructing peptide-like structures. Its chloro substituent offers a handle for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in research settings for drug discovery, especially in oncology and central nervous system therapies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,020.00 |
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| 1g | 10-20 days | ฿3,580.00 |
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2-((tert-Butoxycarbonyl)amino)-4-chlorobenzoic acid
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protected amino groups are required. The Boc-protected amine allows for controlled deprotection during multi-step syntheses, enabling selective reactions without interference. The carboxylic acid functionality provides a site for amide bond formation, making it valuable in constructing peptide-like structures. Its chloro substituent offers a handle for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in research settings for drug discovery, especially in oncology and central nervous system therapies.
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