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2-benzyl-5-methyl-2,5-diaza-bicyclo[2.2.1]heptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59436-76-9

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59436-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59436-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,3 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59436-76:
(7*5)+(6*9)+(5*4)+(4*3)+(3*6)+(2*7)+(1*6)=159
159 % 10 = 9
So 59436-76-9 is a valid CAS Registry Number.

59436-76-9Upstream product

59436-76-9Downstream Products

59436-76-9Relevant academic research and scientific papers

Antifilarial agents. Diazabicyclooctanes and diazabicycloheptanes as bridged analogs of diethylcarbamazine

Sturm,Henry,Thompson,et al.

, p. 481 - 487 (1974)

Twelve analogs of diethylcarbamazine (DEC) were prepared by acylation of 3 and 8 methyl 3,8 diazabicyclo[3.2.1]octane, 2 methyl 2,5 diazabicyclo[2.2.2]octane, and 2 methyl 2,5 diazabicyclo[2.2.1]heptane with diethylcarbamyl chloride, ethyl chloroformate, ethyl isocyanate, and cyclohexanecarbonyl chloride. These compounds are formally derived from DEC in possessing two or one carbon bridges over the piperazine ring. When evaluated against Litomosoides carinii in the gerbil, all compounds strongly suppressed blood microfilaremia levels but did not affect the adult worms. Several compounds were nearly equivalent to DEC in activity. The results are discussed in terms of molecular model studies and receptor site theory.

Diazabicyclooctanes and diazabicycloheptanes

-

, (2008/06/13)

Twelve analogs of diethylcarbamazine as prepared by acylation of 3- and 8-methyl-3,8-diazabicyclo[3.2.1]octane, 2-methyl-2,5-diazabicyclo[2.2.2]octane, and 2-methyl-2,5-diazabicyclo [2.2.1]heptane with diethylcarbamyl chloride, ethyl chloroformate, ethyl isocyanate, and cyclohexanecarbonyl chloride. These compounds are formally derived from diethylcarbamazine in possessing two- or one-carbon bridges over the piperazine ring. The compounds have utility as antifilarial agents and as bronchodilators.

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