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1221279-03-3

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1221279-03-3 Usage

General Description

N-methyl-3-(piperidin-4-yl)benzamide is a chemical compound with the molecular formula C16H21NO. It is a benzamide derivative with a methyl group attached to the nitrogen atom and a piperidine ring attached to the benzene ring. N-methyl-3-(piperidin-4-yl)benzamide is commonly used in research and pharmaceutical applications, where it may be utilized as a building block for the synthesis of other chemical compounds or studied for its potential pharmacological properties. The specific properties and potential uses of N-methyl-3-(piperidin-4-yl)benzamide may vary depending on the intended application, and further research and testing may be required to fully understand its characteristics and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1221279-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,2,7 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1221279-03:
(9*1)+(8*2)+(7*2)+(6*1)+(5*2)+(4*7)+(3*9)+(2*0)+(1*3)=113
113 % 10 = 3
So 1221279-03-3 is a valid CAS Registry Number.

1221279-03-3Relevant articles and documents

Design and synthesis of a new class of malonyl-CoA decarboxylase inhibitors with anti-obesity and anti-diabetic activities

Tang, Haifeng,Yan, Yan,Feng, Zhe,De Jesus, Reynalda K.,Yang, Lihu,Levorse, Dorothy A.,Owens, Karen A.,Akiyama, Taro E.,Bergeron, Raynald,Castriota, Gino A.,Doebber, Thomas W.,Ellsworth, Kenneth P.,Lassman, Michael E.,Li, Cai,Wu, Margaret S.,Zhang, Bei B.,Chapman, Kevin T.,Mills, Sander G.,Berger, Joel P.,Pasternak, Alexander

scheme or table, p. 6088 - 6092 (2010/11/18)

A new series of thiazole-substituted 1,1,1,3,3,3-hexafluoro-2-propanols were prepared and evaluated as malonyl-CoA decarboxylase (MCD) inhibitors. Key analogs caused dose-dependent decreases in food intake and body weight in obese mice. Acute treatment with these compounds also led to a drop in elevated blood glucose in a murine model of type II diabetes.

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