Tert-Butyl (R)-(2,6-dimethyl-3-oxohept-1-en-4-yl)carbamate

98%

Reagent Code: #238244
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CAS Number 2177287-70-4

science Other reagents with same CAS 2177287-70-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.35 g/mol
Formula C₁₄H₂₅NO₃
thermostat Physical Properties
Boiling Point 350.4±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.964±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of chiral pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for constructing complex molecular architectures where control of three-dimensional structure is critical. Also utilized in research settings to develop new synthetic routes requiring protected amine functionalities with steric hindrance.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,340.00
Tert-Butyl (R)-(2,6-dimethyl-3-oxohept-1-en-4-yl)carbamate
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Used as an intermediate in the synthesis of chiral pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for constructing complex molecular architectures where control of three-dimensional structure is critical. Also utilized in research settings to develop new synthetic routes requ

Used as an intermediate in the synthesis of chiral pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for constructing complex molecular architectures where control of three-dimensional structure is critical. Also utilized in research settings to develop new synthetic routes requiring protected amine functionalities with steric hindrance.

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