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3-benzoyloxy-6-methoxy-1,2,3,4-tetrahydro-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51145-59-6

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51145-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51145-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,4 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51145-59:
(7*5)+(6*1)+(5*1)+(4*4)+(3*5)+(2*5)+(1*9)=96
96 % 10 = 6
So 51145-59-6 is a valid CAS Registry Number.

51145-59-6Relevant academic research and scientific papers

An Alternative Synthesis of 3-Amino-1,2,3,4-tetrahydrocarbazoles

Bird, C. W.,Wee, A. G. H.

, p. 191 - 192 (2007/10/02)

3-Amino-1,2,3,4-tetrahydrocarbazoles are easily prepared from the readily available 3-hydroxy-1,2,3,4-tetrahydrocarbazoles by conversion of the latter to the p-toluene- or methanesulfonate ester, followed by nucleophilic displacement with azide ion.The resulting 3-azido-1,2,3,4-tetrahydrocarbazoles are then catalytically hydrogenated to their 3-amino counterparts.

3-Hydroxy carbazole derivatives

-

, (2008/06/13)

3-(Substituted-amino)-1,2,3,4-tetrahydrocarbazoles are prepared by reacting appropriate 4-substituted-aminocyclohexanones with a phenylhydrazine, by reacting a 3-(sulfonyloxy)-1,2,3,4-tetrahydrocarbazole with an appropriate substituted amine, or by reduction of an appropriate 3-(acylamino)-1,2,3,4-tetrahydrocarbazole. The 3-(substituted-amino)-1,2,3,4-tetrahydrocarbazoles of this invention have analgetic and psychotropic activities. Moreover, certain of these compounds also have antihistaminic activity.

3-Amido-1,2,3,4-tetrahydrocarbazoles

-

, (2008/06/13)

3-(Substituted-amino)-1,2,3,4-tetrahydrocarbazoles are prepared by reacting appropriate 4-substituted-aminocyclohexanones with a phenylhydrazine, by reacting a 3-(sulfonyloxy)-1,2,3,4-tetrahydrocarbazole with an appropriate substituted amine, or by reduction of an appropriate 3-(acylamino)-1,2,3,4-tetrahydrocarbazole. The 3-(substituted-amino)-1,2,3,4-tetrahydrocarbazoles of this invention have analgetic and psychotropic activities. Moreover, certain of these compounds also have antihistaminic activity.

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