6289-62-9 Usage
General Description
The chemical [5-(acetyloxymethyl)-6-bicyclo[2.2.1]hept-2-enyl]methyl acetate is a complex organic compound that contains a bicyclic structure and an acetate functional group. Its molecular formula is C13H18O4 and its molecular weight is 238.28 g/mol. [5-(acetyloxymethyl)-6-bicyclo[2.2.1]hept-2-enyl]methyl acetate is commonly used in the field of organic synthesis and pharmaceutical research. It may have potential applications in the development of new drugs or in the creation of specialized chemical products. However, it is important to note that [5-(acetyloxymethyl)-6-bicyclo[2.2.1]hept-2-enyl]methyl acetate should be handled with care and in accordance with proper safety protocols, as its specific properties and potential hazards are not included in this summary.
Check Digit Verification of cas no
The CAS Registry Mumber 6289-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6289-62:
(6*6)+(5*2)+(4*8)+(3*9)+(2*6)+(1*2)=119
119 % 10 = 9
So 6289-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O4/c1-8(14)16-6-12-10-3-4-11(5-10)13(12)7-17-9(2)15/h3-4,10-13H,5-7H2,1-2H3
6289-62-9Relevant articles and documents
Cyclopentanedi- and tricarboxylic acids as squalene synthase inhibitors: Syntheses and evaluation
Shen, Wang,Garvey, David S.,Cohen, Jerry,Stein, Herman,Rosenberg, Saul H.
, p. 891 - 896 (2007/10/03)
Based on earlier lead squalene synthase inhibitor A-87049 (3) and zaragozic acids, a series of cyclopentanedi- and tricarboxylic acids were synthesized and evaluated against the enzyme. Some exhibited good potency and SAR revealed the importance of conformation and substitution pattern of these synthetic inhibitors.
Enzyme mediated optical resolution of endo-norbornene lactone
Janssen,Klunder,Zwanenburg
, p. 7219 - 7222 (2007/10/02)
The enzymatic resolution of some norbornene esters, -carboxylic acids and -methanols was evaluated. Good results were obtained for the Porcine Pancreatic Lipase (PPL) catalyzed transesterification of norbornene methanols 12 and 13 in methyl acetate. A formal kinetic resolution of endo-norbornene lactone 7 could be achieved through the PPL-catalyzed transesterification of iodolactone 15 in methyl acetate. Both enantiomers of lactone 7 were obtained enantiomerically pure in good overall yields.
