91375-04-1 Usage
General Description
2,5-Pyrrolidinedione, 1-(1-cyclohexen-1-ylmethyl)-, also known as Cyclohexenylmethylpyrrolidinedione, is a chemical compound with the molecular formula C11H15NO2. It is a cyclic ketone derivative and is commonly classified as a pyrrolidinedione. 2,5-Pyrrolidinedione, 1-(1-cyclohexen-1-ylmethyl)- is used in the synthesis of various pharmaceutical and organic compounds due to its reactivity and ability to undergo various chemical reactions. It is also used as a building block for the production of other complex organic molecules. The compound has potential applications in the fields of medicine, biochemistry, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 91375-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91375-04:
(7*9)+(6*1)+(5*3)+(4*7)+(3*5)+(2*0)+(1*4)=131
131 % 10 = 1
So 91375-04-1 is a valid CAS Registry Number.
91375-04-1Relevant academic research and scientific papers
Photochemistry of Succinimides with a Cycloalkenylalkyl Group in the Side Chain. Competitive Norrish Type II and Paterno-Buchi Reactions
Machida, Minoru,Oda, Kazuaki,Kanaoka, Yuichi
, p. 950 - 956 (2007/10/02)
Photolysis of N-succinimides (9c-f) (m>/=2) afforded mainly azepinediones (13c-f) with ring enlargement as the Norrish type II cyclization products.In the case of m=1, spiro-azepinedione derivatives (11a, b) were obtained in addition to tricyclic nitrogen heterocycles (10a, b), the Norrish type II products.These spiro-azepinediones are probably formed via imide imide-oxetanes by the intramolecular Paterno-Buchi reaction of these succinimides in competition with the type II processes.Keywords: N-succinimide; Norrish type II reaction; oxetane formation; azepinedione; spiro compound; photochemistry.
