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2-(4-Chlorophenyl)ethyl cyclopropyl carbinol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52121-68-3

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52121-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52121-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,2 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52121-68:
(7*5)+(6*2)+(5*1)+(4*2)+(3*1)+(2*6)+(1*8)=83
83 % 10 = 3
So 52121-68-3 is a valid CAS Registry Number.

52121-68-3Downstream Products

52121-68-3Relevant academic research and scientific papers

Aryl substituted diketones

-

, (2008/06/13)

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester.

Dialkylaminophenylethyl (or vinyl) cyclopropyl carbinols

-

, (2008/06/13)

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester. The intermediate iodides are prepared by cond

Methylenedioxyphenyl substituted aliphatic diketones

-

, (2008/06/13)

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester.

Aryl substituted ketones

-

, (2008/06/13)

Aryl substituted tertiary carbinols, useful as antiviral agents and insecticides, are prepared by reacting the Grignard reagent derived from an arylalkyl or arylalkenyl iodide with a dialkyl ketone or an alkyl alkenyl ketone; or by reacting an arylalkyl or arylalkenyl ketone with an alkyl- or alkenylmagnesium halide.

Antivital activity of some β diketones. I. Aryl alkyl diketones. In vitro activity against both RNA and DNA viruses

Diana,Salvador,Zalay,et al.

, p. 750 - 756 (2007/10/05)

The discovery that 4 [3 ethyl 6 [(3,4 methylenedioxy)phenyl] 3 hexenyl] 3,5 heptanedione exhibited an in vitro inhibitory effect against equine rhinovirus led to a structure activity study to establish the criteria for optimum activity. Modification of th

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