252891-36-4 Usage
Structure
Carboxylic acid with a cyclohexadiene ring and two methyl groups attached to the first and second carbon atoms
Chirality
Chiral molecule with (1S) designation indicating the specific spatial arrangement of its atoms
Uses
Commonly used as a building block in organic synthesis, found in various chemical reactions and pharmaceutical applications, potential use in the development of new drugs, agrochemicals, and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 252891-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,8,9 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 252891-36:
(8*2)+(7*5)+(6*2)+(5*8)+(4*9)+(3*1)+(2*3)+(1*6)=154
154 % 10 = 4
So 252891-36-4 is a valid CAS Registry Number.
252891-36-4Relevant academic research and scientific papers
Stereospecific palladium-catalyzed decarboxylative C(sp3)- C(sp2) Coupling of 2,5-Cyclohexadiene-1-carboxylic Acid Derivatives with Aryl Iodides
Chou, Chih-Ming,Chatterjee, Indranil,Studer, Armido
supporting information; experimental part, p. 8614 - 8617 (2011/11/05)
Walk on the same side! The title reaction occurs by means of highly stereospecific 1,3-metal migration. The starting carboxylic acids are readily prepared by Birch reduction, and the developed protocol provides an efficient route to enantiomerically pure
