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β-Cyclohexylamino-cis-crotonitril is a chemical compound with the molecular formula C11H16N2. It is a derivative of crotonitrile, which is a conjugated nitrile, and features a cyclohexylamine group attached to the β-position. β-cyclohexylamino-cis-crotonitril is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The cis-configuration indicates that the cyclohexylamine group and the nitrile group are on the same side of the double bond, which can influence its chemical properties and interactions with other molecules. β-Cyclohexylamino-cis-crotonitril is an example of how functional group placement and stereochemistry can significantly affect a compound's behavior and utility in chemical processes.

59333-57-2

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59333-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59333-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,3 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59333-57:
(7*5)+(6*9)+(5*3)+(4*3)+(3*3)+(2*5)+(1*7)=142
142 % 10 = 2
So 59333-57-2 is a valid CAS Registry Number.

59333-57-2Downstream Products

59333-57-2Relevant academic research and scientific papers

One-pot conversion of β-aminocrotononitrile to secondary enaminonitriles including chiral ones - Application to synthesis

Chatterjee,Mishra,Dutta Chowdhury,Mahalanabis, Kumar K.

, p. 1164 - 1170 (2007/10/03)

A highly efficient one-pot conversion of β-aminocrotononitrile to secondary enaminonitriles including chiral ones is described. In contrast to β-aminocrotononitrile, some of these N-substituted β-enaminonitriles on reacting with acid chlorides show a unique preference for C-terminal selection allowing preparation of pyrazoles without separation of regioisomers. In addition, use of secondary enaminonitriles also provided access to pyrazoles that are not obtainable with primary enaminonitriles owing to an exclusive preference for N-terminal selection.

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