3-Cyclohexene-1-carboxylic acid, (1S)-, compd. with (αR)-α-methylbenzenemethanamine (1:1)

Chiral pure 99%

Reagent Code: #44660
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CAS Number 67976-82-3

science Other reagents with same CAS 67976-82-3

blur_circular Chemical Specifications

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Weight 247.33274 g/mol
Formula C₁₅H₂₁NO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a cyclohexene ring and a carboxylic acid group, makes it valuable for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs). The presence of (αR)-α-methylbenzenemethanamine enhances its role in asymmetric synthesis, enabling the formation of specific stereoisomers with high selectivity. This is especially important in the design of drugs where the biological activity is highly dependent on the stereochemistry of the molecule. Additionally, it may be employed in organic synthesis for constructing complex molecules with defined spatial arrangements, contributing to advancements in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿4,752.00
inventory 100g
10-20 days ฿14,112.00

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3-Cyclohexene-1-carboxylic acid, (1S)-, compd. with (αR)-α-methylbenzenemethanamine (1:1)
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a cyclohexene ring and a carboxylic acid group, makes it valuable for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs). The presence of (αR)-α-methylbenzenemethanamine enhances its role in asymmetric synthesis, enabling the formation of specific stereoisomers wit

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a cyclohexene ring and a carboxylic acid group, makes it valuable for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs). The presence of (αR)-α-methylbenzenemethanamine enhances its role in asymmetric synthesis, enabling the formation of specific stereoisomers with high selectivity. This is especially important in the design of drugs where the biological activity is highly dependent on the stereochemistry of the molecule. Additionally, it may be employed in organic synthesis for constructing complex molecules with defined spatial arrangements, contributing to advancements in medicinal chemistry and drug discovery.

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