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N-(2-phenylethyl)-3,4-dimethyl-1,2,5,6-tetrahydropyridine, also known as 2-phenylethyl-3,4-dimethyl-1,2,5,6-tetrahydropyridine, is a chemical compound with the molecular formula C16H21N. It is a derivative of tetrahydropyridine, a heterocyclic compound with a six-membered ring containing four carbon atoms and one nitrogen atom. The structure of N-(2-phenylethyl)-3,4-dimethyl-1,2,5,6-tetrahydropyridine features a phenylethyl group attached to the nitrogen atom, and two methyl groups at the 3rd and 4th positions of the tetrahydropyridine ring. N-(2-phenylethyl)-3,4-dimethyl-1,2,5,6-tetrahydropyridine has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and properties.

1212-45-9

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1212-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1212-45-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1212-45:
(6*1)+(5*2)+(4*1)+(3*2)+(2*4)+(1*5)=39
39 % 10 = 9
So 1212-45-9 is a valid CAS Registry Number.

1212-45-9Upstream product

1212-45-9Relevant academic research and scientific papers

Transformations of 1-phenethyl-1,2,3,6-tetrahydropyridines in the presence of trifluoromethanesulfonic acid

Shadrikova, Vera A.,Popov, Alexander S.,Termelyova, Maria V.,Baimuratov, Marat R.,Klimochkin, Yuri N.

, p. 909 - 914 (2020)

[Figure not available: see fulltext.] 1-Phenethyl-1,2,3,6-tetrahydropyridines undergo intramolecular Friedel–Crafts reaction in trifluoromethanesulfonic acid medium, resulting in the formation of azatricyclic structures. It was shown that the direction of

A Short synthesis of benzomorphane analgesics (±)-Metazocine and (±)-Phenazocine

Singh, Kamal Nain,Singh, Pushpinder,Sharma, Arvind Kumar,Singh, Paramjit,Kessar, Satinder V.

experimental part, p. 3716 - 3720 (2010/12/29)

A three step synthesis of (±)-metazocine and (±)-phenazocine starting with 3,4-lutidine is described. The key step involves Lewis acid promoted lithiation/electrophilic substitution reaction of N-alkyl-3,4-dimethyl- 1,2,5,6- tetrahydropyridine. Copyright

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