6532-17-8 Usage
Chemical structure
The compound has a complex structure that includes a piperazine ring and an indole-2,3-dione moiety.
Hydroxyethyl group
The compound contains a hydroxyethyl group attached to the piperazine ring.
Pharmaceutical applications
The presence of the piperazine moiety suggests potential pharmaceutical applications, as it is a common structural feature in many drugs.
Biological activity
The indole-2,3-dione group is known for its biological activity and has been investigated for its potential therapeutic properties.
Complex molecule
1-[4-(2-HYDROXY-ETHYL)-PIPERAZIN-1-YLMETHYL]-1H-INDOLE-2,3-DIONE is a complex molecule with potential pharmacological significance.
Please note that the information provided is based on the given material and may not be exhaustive. Further research and analysis would be required to fully understand the properties and potential applications of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 6532-17-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6532-17:
(6*6)+(5*5)+(4*3)+(3*2)+(2*1)+(1*7)=88
88 % 10 = 8
So 6532-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H19N3O3/c19-10-9-16-5-7-17(8-6-16)11-18-13-4-2-1-3-12(13)14(20)15(18)21/h1-4,19H,5-11H2/p+2
6532-17-8Relevant articles and documents
New N-Mannich bases obtained from isatin and piperazine derivatives: The synthesis and evaluation of antimicrobial activity
Bogdanov, Andrei V.,Vazykhova, Al'bina M.,Khasiyatullina, Nadezhda R.,Krivolapov, Dmitry B.,Dobrynin, Alexey B.,Voloshina, Alexandra D.,Mironov, Vladimir F.
, p. 25 - 30 (2016/03/22)
A Mannich reaction of isatin with monosubstituted piperazines in the presence of aqueous formaldehyde was used to synthesize new, as well as two previously described derivatives of 1-piperazinomethylisatins, which were further converted to isoindigo derivatives. The antimicrobial activity of the obtained heterocycles was evaluated.
