(R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-methylbutanoic acid

97%

  • Product Code: 50121
  CAS:    89536-85-6
Molecular Weight: 231.29 g./mol Molecular Formula: C₁₁H₂₁NO₄
EC Number: MDL Number: MFCD00076996
Melting Point: Boiling Point: 322°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. This protection is crucial in multi-step organic syntheses, particularly in the production of complex molecules like drugs or bioactive peptides. Additionally, its chiral structure makes it valuable in the preparation of enantiomerically pure compounds, which are essential in the development of specific therapeutic agents. Its application is common in medicinal chemistry and biotechnology for designing and optimizing drug candidates.
Product Specification:
Test Specification
APPEARANCE White to yellow Solid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $29.89
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5.000 10-20 days $124.27
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10.000 10-20 days $248.54
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-
25.000 10-20 days $619.78
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(R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-methylbutanoic acid
This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. This protection is crucial in multi-step organic syntheses, particularly in the production of complex molecules like drugs or bioactive peptides. Additionally, its chiral structure makes it valuable in the preparation of enantiomerically pure compounds, which are essential in the development of specific therapeutic agents. Its application is common in medicinal chemistry and biotechnology for designing and optimizing drug candidates.
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