74484-68-7 Usage
Molecular structure
2-(4-[(2R,6S)-2,6-dimethylpiperidin-1-yl]but-2-yn-1-yloxy)-1H-isoindole-1,3(2H)-dione has a complex molecular structure, which includes a piperidinyl group, a butynyl group, and an oxy-isoindole-dione moiety.
Stereochemistry
The compound has specific stereochemistry with a 2R configuration for the piperidinyl group and a 6S configuration for the butynyl group.
Potential pharmaceutical intermediate
Due to its unique structure and potential biological activities, this compound may be an important pharmaceutical intermediate, which can be used in the synthesis of various drugs.
Biological activities
Although not yet fully understood, the compound's structure suggests that it may have potential biological activities, which could be useful in the development of new medications.
Further research and testing required
To fully understand the properties and potential applications of this compound, additional research and testing are necessary. This includes studying its chemical properties, stability, and reactivity, as well as evaluating its potential therapeutic effects and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 74484-68-7 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 74484-68:
(7*7)+(6*4)+(5*4)+(4*8)+(3*4)+(2*6)+(1*8)=157
157 % 10 = 7
So 74484-68-7 is a valid CAS Registry Number.
74484-68-7Relevant 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.
