109322-12-5 Usage
Chemical class
Hydrazinecarbothioamide derivative
Explanation
Different sources of media describe the Explanation of 109322-12-5 differently. You can refer to the following data:
1. The compound contains a sulfur atom linked to a nitrogen atom in a carbonyl group.
2. A fused aromatic ring system present in the compound.
3. Potential pharmacological activities
Antimicrobial
Anti-cancer
Anti-inflammatory
4. Need for further research
3. To fully understand the pharmacological potential of this compound and its possible applications in medicine.
Structural feature
Indoloquinoxaline moiety
Check Digit Verification of cas no
The CAS Registry Mumber 109322-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,2 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109322-12:
(8*1)+(7*0)+(6*9)+(5*3)+(4*2)+(3*2)+(2*1)+(1*2)=95
95 % 10 = 5
So 109322-12-5 is a valid CAS Registry Number.
109322-12-5Relevant articles and documents
Synthesis of 2/9-Substituted Indophenazin-6-acetic Acid &α-Aryl/methylbenzylidenehydrazides, 4-Aryl-1-(indophenazin-6-methylcarbonyl)-3-thiosemicarbazides and 6-(4-Aryl-5-mercapto-4H-1,2,4-triazol-3-ylmethyl)indophenazines as CNS Active and Antiinflammato
Mohan, Rajiv Ravindra,Agarwal, Rajesh,Misra, V. S.
, p. 1234 - 1237 (2007/10/02)
2/9-Substituted indophenazine-6-acetic acid α-aryl/methylbenzylidenehydrazides (IVa-l) and 4-aryl-1-(2/9-substituted indophenazin-6-methylcarbonyl)-3-thiosemicarbazides (Va-j) have been synthesised by condensing 2/9-substituted indophenazin-6-acetic acid