61885-23-2 Usage
Explanation
The compound consists of 21 carbon atoms, 16 hydrogen atoms, 4 nitrogen atoms, and 5 oxygen atoms.
Explanation
The compound has a ring structure consisting of two interconnected cycles or rings.
Explanation
The compound contains three different functional groups that contribute to its chemical properties and reactivity.
Explanation
The compound has a total of 12 carbon atoms in its structure.
Explanation
Praziquantel, the common name for this chemical, is used as a medication to treat infections caused by certain types of parasitic worms.
Explanation
Praziquantel works by paralyzing the worms, which causes them to release their grip on the body and be expelled in the stool.
Explanation
Praziquantel is specifically effective against infections caused by these types of parasites.
Explanation
The World Health Organization considers Praziquantel to be an essential medicine, meaning it is crucial for a basic health system.
Structure
Bicyclic
Functional groups
Two methyl groups, a nitro group, and a carbonitrile group
Total carbon atoms
12
Medicinal use
Treatment of parasitic worm infections
Mode of action
Paralyzes the worms
Commonly used for
Infections caused by Schistosoma and liver flukes
World Health Organization status
Essential medicine
Check Digit Verification of cas no
The CAS Registry Mumber 61885-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,8 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61885-23:
(7*6)+(6*1)+(5*8)+(4*8)+(3*5)+(2*2)+(1*3)=142
142 % 10 = 2
So 61885-23-2 is a valid CAS Registry Number.
61885-23-2Relevant academic research and scientific papers
Pyrimidine Derivatives and Related Compounds. Part 36. Nucleophilic Addition Reaction of a Cyanide Ion to 6-Substituted 1,3-Dimethyl-5-nitrouracils. Synthesis of 5,6-Dihydrouracil and 5,6-Dihydrocyclothymine Derivatives
Hirota, Kosaku,Yamada, Yoshihiro,Asao, Tetsuji,Senda, Shigeo
, p. 1896 - 1899 (2007/10/02)
6-Substituted 1,3-dimethyl-5-nitrouracils (3a-c) react with potassium cyanide to dive stereospecifically the 6-cyano-5-nitro-5,6-dihydrouracils (4a-c).Reaction of 6-bromomethyl-1,3-dimethyl-5-nitrouracil (7) with potassiun cyanide gives 6-cyano-1,3-dimeth
