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1-Ethyl-5-methyl-1,2,3,6-tetrahydropyridine is a chemical compound belonging to the class of tetrahydropyridines, which are cyclic compounds with a six-membered ring structure. This specific compound is characterized by the presence of an ethyl group at the 1-position and a methyl group at the 5-position, with the remaining carbon atoms being part of the saturated ring. It is an organic molecule with the molecular formula C8H15N, and it is a colorless liquid at room temperature. 1-ethyl-5-methyl-1,2,3,6-tetrahydropyridine has potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. However, it is important to note that the compound may have neurotoxic effects, as it is structurally similar to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), a known neurotoxin. As a result, caution should be exercised when handling and using this chemical, and further research is needed to fully understand its properties and potential applications.

5562-36-7

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5562-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5562-36-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5562-36:
(6*5)+(5*5)+(4*6)+(3*2)+(2*3)+(1*6)=97
97 % 10 = 7
So 5562-36-7 is a valid CAS Registry Number.

5562-36-7Relevant academic research and scientific papers

A Biomimetic Approach to the Manzamine Alkaloids; Model Studies

Baldwin, Jack E.,Claridge, Tim D. W.,Heupel, Florian A.,Whitehead, Roger C.

, p. 7829 - 7832 (1994)

An approach to the manzamine alkaloids based on a biogenetic theory has been investigated using a simple model system and the key cycloaddition step has been accomplished in moderate yield.

A novel Diels-Alder approach to hydroisoquinolines

Baldwin, Jack E.,Spring, David R.,Whitehead, Roger C.

, p. 5417 - 5420 (2007/10/03)

A synthetic approach to functionalised hydroisoquinoline rings, using dihydropyridinium ions as dienophiles in the Diels-Alder reaction, is described.

An approach to the manzamine alkaloids modelled on a biogenetic theory

Baldwin, Jack E.,Bischoff, Laurent,Claridge, Tim D. W.,Heupel, Florian A.,Spring, David R.,Whitehead, Roger C.

, p. 2271 - 2290 (2007/10/03)

Improved conditions for the preparation of 17 are reported together with the synthesis of an advanced intermediate 38 en route to keramaphidin B, a plausible biogenetic precursor to the manzamines.

A biomimetic approach to the manzamine alkaloids

Baldwin, Jack E.,Claridge, Tim D. W.,Culshaw, Andrew J.,Heupel, Florian A.,Smrckova, Svatava,Whitehead, Roger C.

, p. 6919 - 6922 (2007/10/03)

Results from model studies of a synthetic approach to the manzamine alkaloids based on a biogenetic theory are reported together with the synthesis of a plausible biogenetic precursor to these alkaloids.

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