(1R,2R)-N-Boc-2-aminocyclohexanol

97%

  • Product Code: 70794
  CAS:    155975-19-2
Molecular Weight: 215.3 g./mol Molecular Formula: C₁₁H₂₁NO₃
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: (1R,2R)-N-Boc-2-aminocyclohexanol is widely used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, particularly in the development of drugs targeting specific biological pathways. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling further functionalization of the molecule. It is commonly employed in the synthesis of complex natural products, peptidomimetics, and other bioactive molecules. Additionally, it serves as an intermediate in the production of catalysts and ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions.
Product Specification:
Test Specification
APPEARANCE White to off-white 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 ฿1,160.00
+
-
5.000 10-20 days ฿4,880.00
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-
25.000 10-20 days ฿19,900.00
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-
(1R,2R)-N-Boc-2-aminocyclohexanol
(1R,2R)-N-Boc-2-aminocyclohexanol is widely used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, particularly in the development of drugs targeting specific biological pathways. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling further functionalization of the molecule. It is commonly employed in the synthesis of complex natural products, peptidomimetics, and other bioactive molecules. Additionally, it serves as an intermediate in the production of catalysts and ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions.
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