168021-79-2 Usage
Uses
Used in Pharmaceutical Industry:
1,3-Benzenedisulfonic acid, 4-[[(1,1-dimethylethyl)oxidoimino]methyl]-, disodium salt is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and functional groups can be utilized to create new drugs with potential therapeutic effects.
Used in Chemical Research:
1,3-BENZENEDISULFONIC ACID, 4-[[(1,1-DIMETHYLETHYL)OXIDOIMINO]METHYL]-,DISODIUM SALT is also used in chemical research as a starting material or reagent in the development of new chemical entities. Its properties can be explored for potential applications in various chemical reactions and processes.
Used in Environmental Applications:
1,3-Benzenedisulfonic acid, 4-[[(1,1-dimethylethyl)oxidoimino]methyl]-, disodium salt can be employed in environmental applications, such as water treatment or soil remediation, due to its ability to interact with various contaminants and pollutants.
Used in Material Science:
1,3-BENZENEDISULFONIC ACID, 4-[[(1,1-DIMETHYLETHYL)OXIDOIMINO]METHYL]-,DISODIUM SALT's unique structure and properties can be utilized in the development of new materials with specific characteristics, such as improved conductivity, stability, or reactivity. This can be particularly useful in the fields of electronics, energy storage, or catalysis.
Biological Activity
Free radical trapping agent. Reduces infarct size and preserves brain function in several animal models of acute ischemic stroke. Neuroprotectant.
Biochem/physiol Actions
Originally characterized for its NO-mimicking activity in preventing peroxynitrite formation and in vivo neuroprotective efficacy in animal models of cerebral ischemia (100 mg/kg i.v. in rabbits; 30-60 mg/kg plus 30-60 mg/kg/h i.v. or 50 mg/kg plus 8.8 mg/kg/h s.c. in rats; 28 mg/kg plus 16 mg/kg/h i.v. in monkeys), OKN-007 (HPN-07, NXY-059) is an orally available α-phenyl-tert-butylnitrone (PBN) derivative that is also shown to exhibit sulfatase 2 (SULF2) inhibitory activity and anticancer efficacy both in cultures (effective conc. 170-200 μM in Huh7 heptoma cultures) and in several rodent glioma models in vivo (C6, RG2, and GL261; 75 mg/kg/day for rats and 168 mg/kg/day for mice via drinking water).
references
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Check Digit Verification of cas no
The CAS Registry Mumber 168021-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,0,2 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 168021-79:
(8*1)+(7*6)+(6*8)+(5*0)+(4*2)+(3*1)+(2*7)+(1*9)=132
132 % 10 = 2
So 168021-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO7S2.2Na/c1-11(2,3)12(13)7-8-4-5-9(20(14,15)16)6-10(8)21(17,18)19;;/h4-7H,1-3H3,(H,14,15,16)(H,17,18,19);;/q;2*+1/p-2/b12-7-;;
