17351-07-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
(1S,2R)-Cyclohexane-1,2-dicarboxylic acid diethyl ester serves as a crucial building block in the synthesis of an array of pharmaceuticals and agrochemicals. Its specific stereochemistry and ester functionality contribute to the creation of complex molecules with targeted biological activities.
Used as a Solvent in Chemical Reactions:
In the realm of chemical reactions, (1S,2R)-Cyclohexane-1,2-dicarboxylic acid diethyl ester is utilized as a solvent. Its ability to dissolve a wide range of substances makes it a versatile component in various chemical processes, facilitating reactions that require a stable and compatible medium.
Used as a Plasticizer in Polymer Production:
(1S,2R)-Cyclohexane-1,2-dicarboxylic acid diethyl ester is employed as a plasticizer, particularly in the manufacturing of polyvinyl chloride (PVC) and other polymers. It enhances the flexibility and workability of these materials, allowing for a broader range of applications in products such as pipes, films, and cables.
Used in Organic Synthesis for Creating Diverse Compounds:
In the field of organic synthesis, (1S,2R)-Cyclohexane-1,2-dicarboxylic acid diethyl ester is a valuable precursor for creating a multitude of compounds with distinct properties and functionalities. Its reactivity and structural features make it suitable for the development of new chemical entities for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17351-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,5 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17351-07:
(7*1)+(6*7)+(5*3)+(4*5)+(3*1)+(2*0)+(1*7)=94
94 % 10 = 4
So 17351-07-4 is a valid CAS Registry Number.
17351-07-4Relevant academic research and scientific papers
Synthesis of 1,4-Cyclohexanedimethanol, 1,4-Cyclohexanedicarboxylic Acid and 1,2-Cyclohexanedicarboxylates from Formaldehyde, Crotonaldehyde and Acrylate/Fumarate
Hu, Yancheng,Zhao, Zhitong,Liu, Yanting,Li, Guangyi,Wang, Aiqin,Cong, Yu,Zhang, Tao,Wang, Feng,Li, Ning
supporting information, p. 6901 - 6905 (2018/06/04)
Valuable polyester monomers and plasticizers—1,4-cyclohexanedimethanol (CHDM), 1,4-cyclohexanedicarboxylic acid (CHDA), and 1,2-cyclohexanedicarboxylates—have been prepared by a new strategy. The synthetic processes involve a proline-catalyzed formal [3+1+2] cycloaddition of formaldehyde, crotonaldehyde, and acrylate (or fumarate). CHDM is produced after a subsequent hydrogenation step over a commercially available Cu/Zn/Al catalyst and a one-pot hydrogenation/oxidation/hydrolysis process yields CHDA, whereas 1,2-cyclohexanedicarboxylate is obtained by a Pd/C-catalyzed tandem decarbonylation/hydrogenation step.
