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(+/-)-4-Methylnicotine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65556-02-7

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65556-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65556-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,5 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65556-02:
(7*6)+(6*5)+(5*5)+(4*5)+(3*6)+(2*0)+(1*2)=137
137 % 10 = 7
So 65556-02-7 is a valid CAS Registry Number.

65556-02-7Downstream Products

65556-02-7Relevant academic research and scientific papers

THE RADICAL AND ORGANOMETALLIC METHYLATION OF NICOTINE AND NICOTINE N-OXIDE

Secor, Henry V.,Chavdarian, Charles G.,Seeman, Jeffrey I.

, p. 3151 - 3154 (1981)

2-Methylnicotine is a major product in the reaction nicotine with methyllithium and methyl radical, in addition to the previously reported 4- and 6-methylnicotines.The reaction of nicotine N-oxide with methylmagnesium bromide furnishes both 2- and 6-methylnicotine.

Organometallic Methylation of Nicotine and Nicotine N-Oxide. Rection Pathways and Racemization Mechanisms

Seeman, Jeffrey I.,Secor, Henry V.,Howe, Charles R.,Chavdarian, Charles G.,Morgan, Larry W.

, p. 4899 - 4904 (2007/10/02)

The reaction of nicotine with methyllithium leads to 2-methylnicotine as a major product in addition to the previously reported 4- and 6-methylnicotines.The reaction of nicotine N-oxide with methylmagnesium bromide furnishes both 2- and 6-methylnicotine.The product composition of these reactions is strongly dependent on the experimental conditions; the effects of solvent, temperature, and relative reagent concentration are presented.The methyllithium reactions lead to partially racemized methylnicotines, and the recovered nicotine is often nearly optically pure.Independently, (S)-(-)-6-methylnicotine was treated with methyllithium and was recovered with complete retention of optical activity.These results suggest that loss of optical purity in the formation of methylnicotines in these methyllithium reactions occurs during the reaction itself and is not due either to racemization of the starting material or to subsequent racemization of the initially formed product.

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