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Piperidine, 2-(2-cyclohexylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51523-85-4

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51523-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51523-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,2 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51523-85:
(7*5)+(6*1)+(5*5)+(4*2)+(3*3)+(2*8)+(1*5)=104
104 % 10 = 4
So 51523-85-4 is a valid CAS Registry Number.

51523-85-4Upstream product

51523-85-4Relevant academic research and scientific papers

1-Acyl-3-(amino-lower-alkyl)indoles

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, (2008/06/13)

1-Acyl-3-(amino-lower-alkyl)indoles, useful as anti-inflammatory agents, are prepared either by acylation of a 3-(amino-lower-alkyl)indole; by Fisher indole synthesis from an N'-acylphenylhydrazine and an amino-lower-alkanone; by alkylation of an amine with a 1-acyl-3-(halo-lower-alkyl)indole; or by reductive alkylation of a 1-acyl-3-indole-lower-alkylcarboxaldehyde.

3-(Piperidino-lower-alkyl)-indoles

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, (2008/06/13)

1-Acyl-3-(amino-lower-alkyl)indoles, useful as anti-inflammatory agents, are prepared either by acylation of a 3-(amino-lower-alkyl)indole; by Fisher indole synthesis from an N'-acylphenylhydrazine and an amino-lower-alkanone; by alkylation of an amine with a 1-acyl-3-(halo-lower-alkyl)indole; or by reductive alkylation of a 1-acyl-3-indole-lower-alkylcarboxaldehyde.

Phenyl-lower-alkylamines

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, (2008/06/13)

Phenyl-lower-alkylamines having anti-inflammatory activity are prepared either by reductive alkylation of an amine with a phenyl-lower-alkanaldehyde; by condensation of a phenyl-lower-alkanaldehyde with a secondary amine, conversion of the resulting phenylvinylamine to the corresponding iminium salt, and reduction of the latter with an alkali metal borohydride; or by reaction of a phenyl-lower-alkanoyl halide with an amine and reduction of the resulting amide with a reagent effective to reduce an amide to an amine.

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