Quality Control of 7-Iodoisobenzofuran-1(3H)-oneOn September 30, 1988 ,《The internal steric push-effect: its consequences on the reactivity of carbonyl functions in 3-substituted phthalic anhydrides》 was published in Spectroscopy Letters. The article was written by Kayser, Margaret M.. The article contains the following contents:
The 13C NMR for a number of 3-substituted phthalic anhydrides and corresponding lactones were measured. Substituent effects were discussed. MM2 calculations for several 3-substituted phthalic anhydrides predict that the substituent and the neighboring carbonyl group remain coplanar and within the plane of the aromatic ring. To alleviate the imposed crowding, there is an in-plane distortion of the bond angle of the substituent and the carbonyl function. The observed angle of distortion increases with increasing steric demand of the substituent, in agreement with repulsive van der Waals interaction between those two groups. Diminished reactivity of the ortho carbonyl groups vis-a-vis nucleophiles in 3-substituted phthalic anhydrides may be linked to the internal steric push-effect which causes the displacement of electrons in the CO bond from O to C. The experimental process involved the reaction of 7-Iodoisobenzofuran-1(3H)-one(cas: 105694-46-0Quality Control of 7-Iodoisobenzofuran-1(3H)-one)
7-Iodoisobenzofuran-1(3H)-one(cas: 105694-46-0) belongs to benzofurans.Quality Control of 7-Iodoisobenzofuran-1(3H)-oneBenzofurans containing one furan ring that have been implicated as psychoactive recreational drugs include 6-(2-aminopropyl)benzofuran (6-APB), 5-(2-aminopropyl)benzofuran (5-APB), 5-(2-ethylaminopropyl)benzofuran (5-EAPB), and 5-methylaminopropylbenzofuran (5-MAPB).
Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem