62251-96-1 Usage
Description
(1S,2S)-2-ethyl-1-([(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-inden-4-yl]carbonylamino)cyclopropanecarboxylic acid is a complex organic compound characterized by a cyclopropane ring and a carboxylic acid functional group. It features a carbonyl group and an amino group attached to the cyclopropane ring, along with an intricate indenyl group. (1S,2S)-2-ethyl-1-([(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-inden-4-yl]carbonylamino)cyclopropanecarboxylic acid's structural complexity and the presence of a cyclopropane ring, which is known to be associated with biological activity in some compounds, suggest potential pharmaceutical applications. Further research is required to explore the specific properties and potential uses of this compound.
Uses
Used in Pharmaceutical Industry:
(1S,2S)-2-ethyl-1-([(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-inden-4-yl]carbonylamino)cyclopropanecarboxylic acid is used as a potential pharmaceutical candidate due to its structural complexity and the presence of a cyclopropane ring, which has been associated with biological activity in some compounds. (1S,2S)-2-ethyl-1-([(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-inden-4-yl]carbonylamino)cyclopropanecarboxylic acid's specific properties and potential uses in the pharmaceutical industry need to be determined through further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 62251-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,5 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62251-96:
(7*6)+(6*2)+(5*2)+(4*5)+(3*1)+(2*9)+(1*6)=111
111 % 10 = 1
So 62251-96-1 is a valid CAS Registry Number.
62251-96-1Relevant articles and documents
Total syntheses of coronatines by exo-selective Diels-Alder reaction and their biological activities on stomatal opening
Okada, Masahiro,Ito, Satoko,Matsubara, Akira,Iwakura, Izumi,Egoshi, Syusuke,Ueda, Minoru
experimental part, p. 3065 - 3073 (2011/02/25)
The natural phytotoxin coronatine, which is composed of two individual parts, coronafacic acid and coronamic acid, exhibits various promising biological activities similar to jasmonic acid. Interestingly, coronatine induces stomatal opening involving the swelling of guard cells in which jasmonic acid is not involved as an endogenous regulator. We established syntheses of four stereoisomers of coronatine employing the exo-selective Diels-Alder reaction as a key step. Remarkable differences in stomatal opening activity were observed between enantiomers of coronatine. This result strongly suggests that the stereo structure of coronatine is very important for its stomatal opening activity. In addition, SAR studies suggested that coronatine operates as a molecular mimic of jasmonyl-l-isoleucine in plant guard cells.
Asymmetric total syntheses of (+)-coronafacic acid and (+)-coronatine
Toshima, Hiroaki,Nara, Shinji,Ichihara, Akitami
, p. 752 - 753 (2007/10/03)
An asymmetric total synthesis of (+)-coronafacic acid, starting from (R)-(+)-4-acetoxy-2-cyclopen-1-one as a chiral source, was accomplished. Construction of the 1-hydrindanone framework was carried out by using intramolecular 1,6-conjugate addition as the key step. Coupling between (+)-coronafacic acid and protected coronamic acid, and subsequent deprotection provided (+)-coronatine. This is the first asymmetric total synthesis of (+)-coronatine.
