tert-Butyl 3-Hydroxypropanoate

98%

  • Product Code: 149682
  CAS:    59854-11-4
Molecular Weight: 146.18 g./mol Molecular Formula: C₇H₁₄O₃
EC Number: MDL Number: MFCD04974574
Melting Point: Boiling Point: 79.0 - 80.0 °C at 11 mmHg (lit.)
Density: 0.990 g/mL at 20 °C (lit.) Storage Condition: Room temperature
Product Description: Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its hydroxyl and ester functional groups allow for selective reactions, making it valuable in the preparation of active pharmaceutical ingredients (APIs). Commonly employed in prodrug design, where the ester group can be hydrolyzed in vivo to release the active compound. Also utilized in the synthesis of polymers and biodegradable materials due to its ability to participate in ring-opening polymerization and other condensation reactions. Its stability and reactivity profile make it suitable for multi-step synthetic routes requiring protection and deprotection strategies.
Product Specification:
Test Specification
Appearance liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size Availability Price Quantity
250mg 10-20 days ฿5,200.00
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-
1g 10-20 days ฿11,920.00
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-
5g 10-20 days ฿48,010.00
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-
bulk 10-20 days ฿0.00
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-
tert-Butyl 3-Hydroxypropanoate
Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its hydroxyl and ester functional groups allow for selective reactions, making it valuable in the preparation of active pharmaceutical ingredients (APIs). Commonly employed in prodrug design, where the ester group can be hydrolyzed in vivo to release the active compound. Also utilized in the synthesis of polymers and biodegradable materials due to its ability to participate in ring-opening polymerization and other condensation reactions. Its stability and reactivity profile make it suitable for multi-step synthetic routes requiring protection and deprotection strategies.
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