(1R,2R)-2-Aminocyclohexanol

97%

Reagent Code: #68242
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CAS Number 931-16-8

science Other reagents with same CAS 931-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115 g/mol
Formula C₆H₁₃NO
badge Registry Numbers
MDL Number MFCD08061325
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

(1R,2R)-2-Aminocyclohexanol is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the creation of beta-blockers and other cardiovascular medications. Additionally, it is employed in asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. This compound is also explored in the field of organic chemistry for the preparation of complex molecules with specific chiral centers, aiding in the study of stereochemical effects on biological activity.

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Test Parameter Specification
Purity 96.5-100%
Appearance colorless liquid

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿8,900.00
inventory 1g
10-20 days ฿600.00
inventory 5g
10-20 days ฿2,120.00

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(1R,2R)-2-Aminocyclohexanol
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(1R,2R)-2-Aminocyclohexanol is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the creation of beta-blockers and other cardiovascular medications. Additionally, it is employed in asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. This compound is also explored in the field of organic chemistry
(1R,2R)-2-Aminocyclohexanol is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the creation of beta-blockers and other cardiovascular medications. Additionally, it is employed in asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. This compound is also explored in the field of organic chemistry for the preparation of complex molecules with specific chiral centers, aiding in the study of stereochemical effects on biological activity.
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