(R)-a-Hydroxy-cyclohexanepropanoic acid

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Reagent Code: #37632
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CAS Number 156469-00-0

science Other reagents with same CAS 156469-00-0

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Weight 172.2215 g/mol
Formula C₉H₁₆O₃
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MDL Number MFCD17171007
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(R)-α-Hydroxy-cyclohexanepropanoic acid is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, ensuring high specificity and efficacy in therapeutic applications. Additionally, it is employed in the development of fine chemicals and agrochemicals, where its chiral properties enhance the performance and safety of the end products. In research, it is used as a building block for complex organic molecules, aiding in the study of stereochemistry and reaction mechanisms. Its role in asymmetric synthesis is particularly valuable for creating compounds with precise three-dimensional structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,410.00

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(R)-a-Hydroxy-cyclohexanepropanoic acid
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(R)-α-Hydroxy-cyclohexanepropanoic acid is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, ensuring high specificity and efficacy in therapeutic applications. Additionally, it is employed in the development of fine chemicals and agrochemicals, where its chiral properties enhance the performance and safety of the end products. In research, it is used as a building block f

(R)-α-Hydroxy-cyclohexanepropanoic acid is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, ensuring high specificity and efficacy in therapeutic applications. Additionally, it is employed in the development of fine chemicals and agrochemicals, where its chiral properties enhance the performance and safety of the end products. In research, it is used as a building block for complex organic molecules, aiding in the study of stereochemistry and reaction mechanisms. Its role in asymmetric synthesis is particularly valuable for creating compounds with precise three-dimensional structures.

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