17351-07-4 Usage
General Description
(1S,2R)-Cyclohexane-1,2-dicarboxylic acid diethyl ester is a chemical compound with the molecular formula C14H24O4. It is the diethyl ester of cyclohexanedicarboxylic acid, which is a derivative of cyclohexane. (1S,2R)-Cyclohexane-1,2-dicarboxylic acid diethyl ester is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also used as a solvent in chemical reactions and as a plasticizer in the production of polyvinyl chloride (PVC) and other polymers. Additionally, it has potential applications in the field of organic synthesis, where it can be used to create a variety of other compounds with different properties and functionalities.
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 articles and documents
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.
