20199-04-6 Usage
Uses
Used in Organic Synthesis:
Thiobenzamide-S-oxide is used as a building block in the synthesis of other organic compounds for its chemical structure and reactivity, contributing to the development of new molecules with specific properties.
Used in Pharmaceutical Research:
Thiobenzamide-S-oxide is employed as a research compound in the pharmaceutical industry for its potential pharmacological activities, such as antibacterial and cytotoxic properties, which can be harnessed for the development of new drugs and therapies.
Used in Antibacterial Applications:
In the field of microbiology, thiobenzamide-S-oxide is used as an antibacterial agent, targeting and inhibiting the growth of harmful bacteria, thereby contributing to the development of new antimicrobial treatments.
Used in Cytotoxicity Studies:
In cancer research, thiobenzamide-S-oxide is utilized in cytotoxicity studies to evaluate its potential as an anticancer agent, exploring its ability to selectively target and kill cancer cells while minimizing damage to healthy cells.
Check Digit Verification of cas no
The CAS Registry Mumber 20199-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,9 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20199-04:
(7*2)+(6*0)+(5*1)+(4*9)+(3*9)+(2*0)+(1*4)=86
86 % 10 = 6
So 20199-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NOS/c8-7(10-9)6-4-2-1-3-5-6/h1-5H,8H2
20199-04-6Relevant articles and documents
X-ray diffraction and self condensation reaction of thionicotinamide S-oxide
Corradi, Anna Bonamartini,Boga, Carla,Forlani, Luciano,Sgarabotto, Paolo
, p. 115 - 119 (1999)
Thiobenzamide and thionicotnamide S-oxide were prepared as intermediates in the dimerization of corresponding thioamides to 1,2,4-thiadiazoles and the X-ray crystal structure of thionicotinamide S-oxide water solvate was determined. Crystals belong to orthorhombic Pbca space group with a = 14.129(3), b = 7.299(2), c = 15.277(3)?, and Z = 8. The geometry of the molecule accords well with that found in similar compounds; an intramolecular N-H ? O hydrogen bond is present, while the packing is mainly determined by the hydrogen bond system involving the water molecule and the side-chain of the organic molecule. The contacts between pyridine moieties, stacked along the [010] axis, complete the packing.