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Cyclohexanone, 2-(1-pyrrolidinyl)-, oxime is an organic compound with the chemical formula C10H17NO2. It is a derivative of cyclohexanone, featuring a pyrrolidinyl group at the 2-position and an oxime functional group. Cyclohexanone, 2-(1-pyrrolidinyl)-, oxime is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs. Its structure provides a unique set of chemical properties that can be exploited in chemical reactions, making it a valuable component in the field of organic chemistry.

3542-57-2

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3542-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3542-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3542-57:
(6*3)+(5*5)+(4*4)+(3*2)+(2*5)+(1*7)=82
82 % 10 = 2
So 3542-57-2 is a valid CAS Registry Number.

3542-57-2Relevant academic research and scientific papers

NITROGEN-CONTAINING CYCLOHETERO CYCLOALKYLAMINOARYL DERIVATIVES FOR CNS DISORDERS

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, (2008/06/13)

Certain nitrogen-containing cyclohetero cycloalkylaminoaryl compounds are described for treatment of CNS disorders such as cerebral ischemia, psychotic disorders, convulsions and parkinsonism. Compounds of particular interest are of the formula STR1 wherein R 1 is selected from hydrido, loweralkyl, cycloalkylalkyl of four to six carbon atoms and loweralkenylloweralkyl; wherein each of R 2 and R 3 is independently selected from hydrido and loweralkyl; wherein each of R 4 through R 7, R 10 and R 11 is independently selected from hydrido, hydroxy, loweralkyl, benzyl, phenoxy, benzyloxy and haloloweralkyl; wherein n is a number selected from four through six; wherein p is a number selected from zero through four; wherein q is a number selected from three through five; wherein A is selected from phenyl, naphthyl and thienyl; wherein any of the foregoing A groups can be further substituted with one or more substituents independently selected from hydrido, hydroxy, loweralkyl, loweralkoxy, halo, haloloweralkyl, amino, monoloweralkylamino and diloweralkylamino; or a pharmaceutically acceptable salt thereof.

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