rel-(1R,2R,3S)-2-aminocyclohexane-1,3-diol

95%

Reagent Code: #84781
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CAS Number 38332-12-6

science Other reagents with same CAS 38332-12-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.17 g/mol
Formula C₆H₁₃NO₂
badge Registry Numbers
MDL Number MFCD19203876
thermostat Physical Properties
Melting Point 191.5-193.5 °C
Boiling Point 271.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.214±0.06 g/cm3(Predicted)
Storage 2-8°C, keep away from light, dry and sealed

description Product Description

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antibacterial agents. Its unique stereochemistry makes it a valuable building block for creating molecules that can interact effectively with biological targets. It is also employed in the production of chiral catalysts, which are essential in asymmetric synthesis to produce enantiomerically pure substances. Additionally, it finds application in research and development for studying enzyme inhibition and receptor binding due to its structural similarity to certain natural substrates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,115.00
inventory 250mg
10-20 days ฿20,475.00
inventory 1g
10-20 days ฿40,950.00

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rel-(1R,2R,3S)-2-aminocyclohexane-1,3-diol
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This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antibacterial agents. Its unique stereochemistry makes it a valuable building block for creating molecules that can interact effectively with biological targets. It is also employed in the production of chiral catalysts, which are essential in asymmetric synthesis to produce enantiomerically pure substances. Additionally, it finds application in research and development for s

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antibacterial agents. Its unique stereochemistry makes it a valuable building block for creating molecules that can interact effectively with biological targets. It is also employed in the production of chiral catalysts, which are essential in asymmetric synthesis to produce enantiomerically pure substances. Additionally, it finds application in research and development for studying enzyme inhibition and receptor binding due to its structural similarity to certain natural substrates.

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