7207-97-8 Usage
Description
ARSENIC DIIODO METHANE, also known as Methyldiiodoarsine, is an arsenite metabolite found in wild type CHO cells and in cells deficient in excision repair cross-complementing 1 and 2. It is a highly toxic compound and acts as an inhibitor of Thioredoxin reductase, an enzyme that plays a crucial role in the cell's response to oxidative stress.
Uses
Used in Pharmaceutical Industry:
ARSENIC DIIODO METHANE is used as a research compound for studying the effects of arsenic metabolism and its role in the inhibition of Thioredoxin reductase enzyme. This helps in understanding the potential therapeutic applications of arsenic-based compounds in the treatment of various diseases.
Used in Toxicology Research:
ARSENIC DIIODO METHANE is used as a toxicological agent in research studies to investigate the mechanisms of arsenic toxicity and its impact on cellular processes. This aids in the development of strategies to mitigate the harmful effects of arsenic exposure and to identify potential antidotes for arsenic poisoning.
Safety Profile
Poison by intravenous
route. When heated to decomposition it
emits toxic fumes of As and I-.
Check Digit Verification of cas no
The CAS Registry Mumber 7207-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7207-97:
(6*7)+(5*2)+(4*0)+(3*7)+(2*9)+(1*7)=98
98 % 10 = 8
So 7207-97-8 is a valid CAS Registry Number.
InChI:InChI=1/CH3AsI2/c1-2(3)4/h1H3
7207-97-8Relevant articles and documents
Reaction of 10-methyl(phenyl)-5,10-dihydrophenarsazine 10-oxides with hydriodic acid
Gavrilov,Karavanov,Musin,Garieva,Musin
, p. 1212 - 1215 (2007/10/03)
We have studied the reaction of 10-methyl(phenyl)-5,10-dihydrophenarsazine 10-oxides with hydriodic acid and we have established the structure of the products by high-resolution mass spectrometry. We have shown that when the methyl group is replaced by a phenyl group in 5,10-dihydrophenarsazine 10-oxides, cleavage of the endocyclic arsenic-carbon bonds occurs. 2004 Springer Science+Business Media, Inc.
