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3-(Pyrrolidin-1-yl)cyclopent-2-en-1-one is a chemical compound with the molecular formula C9H13NO. It is a heterocyclic compound, featuring a cyclopentane ring with a 2-en-1-one functional group and a pyrrolidin-1-yl substituent at the 3-position. 3-(pyrrolidin-1-yl)cyclopent-2-en-1-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is an important intermediate in organic chemistry, particularly in the preparation of complex molecules that require the presence of both a cyclopentane ring and a pyrrolidine moiety. The compound's properties, such as its reactivity and stability, make it a valuable building block in the development of new drugs and other chemical products.

36287-28-2

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36287-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36287-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,8 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36287-28:
(7*3)+(6*6)+(5*2)+(4*8)+(3*7)+(2*2)+(1*8)=132
132 % 10 = 2
So 36287-28-2 is a valid CAS Registry Number.

36287-28-2Downstream Products

36287-28-2Relevant academic research and scientific papers

Gold-catalyzed heterogeneous aerobic dehydrogenative amination of α,β-unsaturated aldehydes to enaminals

Jin, Xiongjie,Yamaguchi, Kazuya,Mizuno, Noritaka

supporting information, p. 455 - 458 (2014/01/23)

Although enaminals (β-enaminals) are very important compounds and have been utilized as useful synthons for various important compounds, they have been synthesized through non-green and/or limited procedures until now. Herein, we have successfully develop

Systematic studies on structure and physiological activity of cyclic α-keto enamines, a novel class of cooling compounds

Ottinger,Soldo,Hofmann

, p. 5383 - 5390 (2007/10/03)

3-Methyl- and 5-methyl-2-(1-pyrrolidinyl)-2-cyclopenten-1-one were recently identified as intense cooling compounds in roasted dark malt. To gain more insights into the molecular requirements of these compounds for imparting a cooling sensation, 26 cyclic α-keto enamine derivatives were synthesized, and their physiological cooling activities were evaluated. Any modification of the amino moiety, the carbocyclic ring size, or incorporation of additional methyl groups led to a significant increase of the cooling threshold. Insertion of an oxygen atom into the 2-cyclopenten-l-one ring, however, increased the cooling activity, e.g., the cooling threshold of the 5-methyl-4-(1-pyrrolidinyl)3(2H)-furanone was found to be 16-fold below the threshold concentration determined for the 3-methyl-2-(1-pyrrolidinyl)-2-cyclopenten-1-one. Shifting the oxygen atom from the 4- into the 5-position of the cyclopentenone ring resulted in a even more drastic increase in cooling activity, e.g., the 4-methyl-3-(1-pyrrolidinyl)-2(5H)-furanone exhibited the strongest cooling effect at the low oral threshold concentration of 0.02-0.06 mmol/L, which is 35-fold below the value determined for (-)-menthol. In contrast to the minty smelling (-)-menthol, most of the α-keto enamines were found to be virtually odorless but impart a sensation of cooling to the oral cavity as well as to the skin, thus illustrating that there is no physiological link between cooling activity and mint-like odors.

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