74484-69-8 Usage
General Description
2-[4-(azepan-1-yl)but-2-ynoxy]isoindole-1,3-dione is a chemical compound with a long and complex name. It contains a unique structure with an isoindole-1,3-dione core and a but-2-ynoxy side chain. The azepan-1-yl group adds a seven-membered ring to the molecule, contributing to its complex and potentially diverse reactivity. 2-[4-(azepan-1-yl)but-2-ynoxy]isoindole-1,3-dione may have potential applications in pharmaceuticals, materials science, or other fields due to its unique structure and potential reactivity. However, further research and testing would be needed to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 74484-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74484-69:
(7*7)+(6*4)+(5*4)+(4*8)+(3*4)+(2*6)+(1*9)=158
158 % 10 = 8
So 74484-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O3/c21-17-15-9-3-4-10-16(15)18(22)20(17)23-14-8-7-13-19-11-5-1-2-6-12-19/h3-4,9-10H,1-2,5-6,11-14H2
74484-69-8Relevant articles and documents
Synthesis and biological evaluation of N-(4-t-amino-2-butynyloxy) and N-(4-t-amino-2-butynyl) phthalimides
Eldeen,Shubber,Musa,et al.
, p. 85 - 88 (2007/10/02)
A series of N-(4-t-amino-2-butynyloxy) and N-(4-t-amino-2-butynyl) phthalimides have been prepared through the Mannich reaction from N-(propargyloxy) phthalimide or N-propargylphthalimide with formaldehyde and various cyclic amines. These compounds have been investigated for blockade of oxotremorine in intact mice, and for their antagonistic activity towards acetylcholine on isolated guinea pig ileal preparations. None of the oxyphthalimido derivatives show oxotremorine antagonistic activity, but all have an acetylcholine antagonistic activity. The phthalimido compounds, on the other hand, have both oxotremorine and acetylcholine antagonistic activity.
