105284-21-7 Usage
General Description
(4E)-4-{(1S,2R,3S,6R)-2-[(3S)-3-cyclohexyl-3-hydroxyprop-1-yn-1-yl]-3-hydroxybicyclo[4.2.0]oct-7-ylidene}butanoic acid is a chemical compound with a complex and unique structure. It contains a butanoic acid group as well as a bicyclo[4.2.0]oct-7-ylidene ring. The compound also has a cyclohexyl group and a propyn-1-yl group, both of which are connected to a hydroxy group. The stereochemistry of the molecule is specified with (1S,2R,3S,6R) configuration. The (4E) in the name indicates that there is a trans double bond between the fourth and fifth carbon atoms. (4E)-4-{(1S,2R,3S,6R)-2-[(3S)-3-cyclohexyl-3-hydroxyprop-1-yn-1-yl]-3-hydroxybicyclo[4.2.0]oct-7-ylidene}butanoic acid may have potential applications in pharmaceuticals, organic synthesis, or other chemical industries due to its unique structure and stereochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 105284-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,8 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105284-21:
(8*1)+(7*0)+(6*5)+(5*2)+(4*8)+(3*4)+(2*2)+(1*1)=97
97 % 10 = 7
So 105284-21-7 is a valid CAS Registry Number.
105284-21-7Relevant articles and documents
Potent Prostacyclin Analogues Based on the Bicyclooctane Ring System
Kluge, Arthur F.,Kertesz, Denis J.,O-Yang, Counde,Wu, Helen Y.
, p. 2860 - 2868 (2007/10/02)
The novel and biologically active prostacyclin mimetics 2 and 29 were prepared in a sequence based on the regioselective opening of epoxide 7 with a lithium acetylide in the presence of boron trifluoride etherate.The regioselectivity of epoxide opening wa
