58684-77-8 Usage
1H-Isoindole-1,3(2H)-dione core
The chemical consists of a core structure of 1H-isoindole-1,3(2H)-dione, which is a bicyclic compound with a five-membered ring fused to a six-membered ring.
3a,4,7,7a-tetrahydro substituent
The chemical has a 3a,4,7,7a-tetrahydro substituent, which indicates the presence of four hydrogen atoms on the isoindole ring.
2-(4-methoxyphenyl) group
The chemical contains a 2-(4-methoxyphenyl) substituent, which is a phenyl ring with a methoxy (CH3O-) group attached to it, located on the second carbon of the tetrahydro substituent.
cis-configuration
The chemical has a cis-configuration, which refers to the spatial arrangement of the substituents on the isoindole ring, with the 2-(4-methoxyphenyl) group and the tetrahydro substituent on the same side of the ring.
Potential applications
The chemical may have potential applications in various fields such as pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 58684-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,8 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58684-77:
(7*5)+(6*8)+(5*6)+(4*8)+(3*4)+(2*7)+(1*7)=178
178 % 10 = 8
So 58684-77-8 is a valid CAS Registry Number.
58684-77-8Relevant academic research and scientific papers
Kamon, Takuma,Irifune, Yayoi,Tanaka, Tetsuaki,Yoshimitsu, Takehiko
, p. 2674 - 2677 (2011)
A novel photochemical C-H carbamoylation of an octahydroisoindole derivative with PhNCO has allowed the authors to provide a unique access to a highly functionalized proline motif from which total synthesis of (±)-kainic acid, a bioactive marine alkaloid, has been accomplished.
