(1R,2R,4R)-2-Acetoxy-4-methylcyclohexanecarboxylic acid

≥95%

Reagent Code: #230727
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CAS Number 1242179-01-6

science Other reagents with same CAS 1242179-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.23 g/mol
Formula C₁₀H₁₆O₄
thermostat Physical Properties
Boiling Point 308.9±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of drugs requiring specific stereochemistry for optimal biological activity. Its functional groups—carboxylic acid and acetoxy—allow for further chemical modifications, making it valuable in creating intermediates for anti-inflammatory or central nervous system agents. The defined stereochemistry (1R,2R,4R) ensures high enantioselectivity in drug synthesis, improving efficacy and reducing unwanted side effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,240.00
inventory 1g
10-20 days ฿42,640.00
(1R,2R,4R)-2-Acetoxy-4-methylcyclohexanecarboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of drugs requiring specific stereochemistry for optimal biological activity. Its functional groups—carboxylic acid and acetoxy—allow for further chemical modifications, making it valuable in creating intermediates for anti-inflammatory or central nervous system agents. The defined stereochemistry (1R,2R,4R) ensures high enantioselectivity in drug synthesis, improving efficacy and reducing unwanted side ef

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of drugs requiring specific stereochemistry for optimal biological activity. Its functional groups—carboxylic acid and acetoxy—allow for further chemical modifications, making it valuable in creating intermediates for anti-inflammatory or central nervous system agents. The defined stereochemistry (1R,2R,4R) ensures high enantioselectivity in drug synthesis, improving efficacy and reducing unwanted side effects.

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