74484-70-1 Usage
Chemical compound
2-[4-(azocan-1-yl)but-2-ynoxy]isoindole-1,3-dione
Core structure
Isoindole-1,3-dione
Attached group
4-(azocan-1-yl)but-2-ynoxy
Derivative of
Isoindole-1,3-dione
Heterocyclic compound with fused ring system
Added flexibility and reactivity from azocan-1-yl and but-2-ynoxy groups
Potential applications in chemical synthesis, material science, or pharmaceutical research
Unique structure with potential functional groups for modifications
Handle with care and follow safety protocols due to potentially reactive nature
Check Digit Verification of cas no
The CAS Registry Mumber 74484-70-1 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, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74484-70:
(7*7)+(6*4)+(5*4)+(4*8)+(3*4)+(2*7)+(1*0)=151
151 % 10 = 1
So 74484-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H22N2O3/c22-18-16-10-4-5-11-17(16)19(23)21(18)24-15-9-8-14-20-12-6-2-1-3-7-13-20/h4-5,10-11H,1-3,6-7,12-15H2
74484-70-1Relevant 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.