93201-85-5 Usage
Heterocyclic compound
Contains both nitrogen and carbon atoms
The structure of this compound includes a ring of atoms with both nitrogen and carbon, making it a heterocyclic compound.
Derivative of imidazoquinoline
A chemical modification of the parent compound
This compound is derived from the parent compound imidazoquinoline, which means it has a similar structure but with some modifications.
Building block in pharmaceutical synthesis
Used to create various pharmaceuticals and organic compounds
This compound serves as a starting material or intermediate in the synthesis of different pharmaceuticals and organic compounds.
Potential biological activity
Being studied for its antiviral and anticancer properties
Research is being conducted to determine if this compound has any beneficial effects against viruses and cancer cells.
Applications in dye and pigment production
Used in the creation of dyes and pigments
This compound has potential uses in the production of dyes and pigments due to its chemical properties.
Organic chemistry applications
Has potential applications in the field of organic chemistry
The compound's unique structure and properties make it a valuable tool for research and development in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 93201-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,0 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93201-85:
(7*9)+(6*3)+(5*2)+(4*0)+(3*1)+(2*8)+(1*5)=115
115 % 10 = 5
So 93201-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H9N3/c1-7-13-10-5-4-9-8(11(10)14-7)3-2-6-12-9/h2-6H,1H3,(H,13,14)
93201-85-5Relevant articles and documents
Studies on the Stability of 2,2,4-Trialkyl-2,3-dihydro-1H-diazepinoquinolines
Reddy, A. Panduranga,Veeranagaiah, V.
, p. 272 - 273 (2007/10/02)
2,2,4-Trialkyl-2,3-dihydro-1H-diazepinoquinolines (I) on treatment with acid or under thermal conditions exclusively result in the formation of 2-methyl-3H-imidazoquinolines (II).However, no change is observed when I is treated with a base under similar conditions.A plausible mechanism for the formation of II as an exclusive product has been explained.
A Facile Synthesis of 2-Substituted Imidazoquinolines
Reddy, A. Pandu Ranga,Veeranagaiah, V.
, p. 673 - 674 (2007/10/02)
Condensation of quinoline-5,6-diamine (II) with aliphatic and aromatic acids under catalytic and thermal conditions results in the corresponding 2-alkyl/aryl-1H-imidazoquinolines (I).
