41138-69-6 Usage
General Description
Methyl (R)-(+)-3-(tert-butyldimethylsil yloxy)-5-oxo-1-cyclopentene-1-heptanoate is a chemical compound that belongs to the class of esters. It is commonly used in organic synthesis and chemical reactions as a building block for creating various types of compounds. METHYL (R)-(+)-3-(TERT-BUTYLDIMETHYLSILYLOXY)-5-OXO-1-CYCLOPENTENE-1-HEPTANOATE has a cyclopentene ring and a heptanoate group, making it a versatile intermediate in the production of pharmaceuticals, fragrances, and other fine chemicals. The tert-butyldimethylsilyloxy group enhances the stability and reactivity of the compound, allowing for precise control in chemical transformations. Overall, this chemical serves as a valuable tool in the field of organic chemistry for the synthesis and modification of complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 41138-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,3 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41138-69:
(7*4)+(6*1)+(5*1)+(4*3)+(3*8)+(2*6)+(1*9)=96
96 % 10 = 6
So 41138-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H34O4Si/c1-19(2,3)24(5,6)23-16-13-15(17(20)14-16)11-9-7-8-10-12-18(21)22-4/h13,16H,7-12,14H2,1-6H3/t16-/m0/s1
41138-69-6Relevant articles and documents
USE OF MEXIPROSTIL IN THE TREATMENT OF INFLAMMATORY BOWEL DISEASE AND/OR OF IRRITABLE BOWEL SYNDROME
-
Paragraph 0068, (2013/08/15)
The invention relates to the use of mexiprostil in the treatment and/or prevention of inflammatory bowel disease and of irritable bowel syndrome, to the combinations of mexiprostil with other drugs, and also to a novel method for the synthesis of mexipros
Total synthesis of isoprostanes via the two-component coupling process
Rodríguez, Ana R.,Spur, Bernd W.
, p. 4575 - 4579 (2007/10/03)
A short total synthesis of isoprostanes has been achieved using a two-component coupling process combined with a diastereoselective protonation under reagent control. The F1-isoprostanes were easily obtained by stereoselective reduction of the C-9 keto group.
Synthesis and antiviral activity of prostaglandin-J1 methyl ester
Roberts, Stanley M.,Gabriella Santoro,Guyot, Thierry
, p. 2437 - 2438 (2007/10/03)
A prostagIandin-F, a methyl ester derivative (12) possessing three different protecting groups on the hydroxy units was prepared so as to allow selective removal of the group attached to the 11-OH group. Compound (12) was converted into prostaglandin-J, m