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Propanamide, N-cyclohexyl-3-mercapto-, also known as 3-Mercaptopropionamide or N-Cyclohexyl-3-mercaptopropanamide, is an organic compound with the chemical formula C9H17NS. It is a colorless to pale yellow liquid with a molecular weight of 175.30 g/mol. Propanamide, N-cyclohexyl-3-mercapto- is characterized by the presence of a cyclohexyl group attached to the nitrogen atom of a propanamide (propionic acid amide) structure, and a thiol (mercapto) group attached to the third carbon. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is important to handle Propanamide, N-cyclohexyl-3-mercapto- with care, following proper safety protocols.

2935-89-9

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2935-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2935-89-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2935-89:
(6*2)+(5*9)+(4*3)+(3*5)+(2*8)+(1*9)=109
109 % 10 = 9
So 2935-89-9 is a valid CAS Registry Number.

2935-89-9Downstream Products

2935-89-9Relevant academic research and scientific papers

Scale up of a ritter reaction

Chang, Sou-Jen

, p. 232 - 234 (1999)

The Ritler reaction of secondary or tertiary alcohols with acrylonitrile provides easy access to acrylamides which would otherwise be difficult to prepare. A safe procedure for conducting this reaction is described.

Process for preparing isothiazolones

-

, (2008/06/13)

The process involves the cofeeding of an acrylonitrile with an appropriate alcohol or its equivalent and a strong acid to form an acrylamide which is thiolated to form a mercapto-propionamide which is halogenated to afford the desired biocidally active isothiazolones. This invention relates to a novel process for preparing N-substituted 3-mercaptopropionamides, an intermediate in the preparation of isothiazolones.

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