(1R,2R)-Cyclohexane-1,2-dicarboxylic acid

98.0%

Reagent Code: #229849
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CAS Number 46022-05-3

science Other reagents with same CAS 46022-05-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₈H₁₂O₄
badge Registry Numbers
MDL Number MFCD00062973
thermostat Physical Properties
Melting Point 184 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for developing enantiomerically pure drugs. Its rigid cyclohexane backbone and two carboxylic acid groups allow it to act as a versatile ligand or co-monomer in catalysis and polymer chemistry. It is also employed in the preparation of specialty esters and amides for use in agrochemicals and fine chemicals. Due to its stereochemistry, it helps induce chirality in target molecules during synthetic transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿174.00
5g
10-20 days ฿360.00
25g
10-20 days ฿1,220.00
100g
10-20 days ฿4,840.00
(1R,2R)-Cyclohexane-1,2-dicarboxylic acid
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Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for developing enantiomerically pure drugs. Its rigid cyclohexane backbone and two carboxylic acid groups allow it to act as a versatile ligand or co-monomer in catalysis and polymer chemistry. It is also employed in the preparation of specialty esters and amides for use in agrochemicals and fine chemicals. Due to its stereochemistry, it helps induce chirality in target molecules during synthetic transformat
Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for developing enantiomerically pure drugs. Its rigid cyclohexane backbone and two carboxylic acid groups allow it to act as a versatile ligand or co-monomer in catalysis and polymer chemistry. It is also employed in the preparation of specialty esters and amides for use in agrochemicals and fine chemicals. Due to its stereochemistry, it helps induce chirality in target molecules during synthetic transformations.
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