109322-17-0 Usage
Structure
Hydrazinecarbothioamide derivative
The compound is derived from hydrazinecarbothioamide, which is a chemical structure containing a hydrazine group (-NHNH-) and a thioamide group (-CSNH2).
Brominated indoloquinoxalinyl acetyl group
The compound contains a 9-bromo-6H-indolo[2,3-b]quinoxalin-6-yl group, which is an indoloquinoxalinyl acetyl group with a bromine atom attached at the 9-position.
4-methylphenyl hydrazinecarbothioamide group
The compound also contains a 4-methylphenyl group, which is a phenyl group (a six-membered aromatic ring with hydrogen atoms) with a methyl group (-CH3) attached at the 4-position, connected to the hydrazinecarbothioamide group.
Potential applications
Pharmaceutical and medicinal chemistry
Due to its structural features and potential biological activities, 2-[(9-bromo-6H-indolo[2,3-b]quinoxalin-6-yl)acetyl]-N-(4-methylphenyl)hydrazinecarbothioamide may have potential applications in the pharmaceutical and medicinal chemistry fields.
Further investigation needed
The exact properties and uses of this compound would need to be determined through additional experimentation and testing.
Check Digit Verification of cas no
The CAS Registry Mumber 109322-17-0 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 109322-17:
(8*1)+(7*0)+(6*9)+(5*3)+(4*2)+(3*2)+(2*1)+(1*7)=100
100 % 10 = 0
So 109322-17-0 is a valid CAS Registry Number.
109322-17-0Relevant 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