1207-71-2 Usage
Uses
Used in Pharmaceutical Industry:
PHENOTHIAZINE-5-OXIDE is used as an intermediate in the synthesis of Phenothiazine S,S-Dioxide, which is a key component in the development of antipsychotic and antihistaminic drugs. Its presence in the synthesis process contributes to the production of these essential medications, helping to treat various mental health conditions and allergies.
Used in Chemical Research:
PHENOTHIAZINE-5-OXIDE can be utilized as a research compound in the field of chemistry, particularly in the study of Phenothiazine derivatives and their potential applications. Its unique chemical properties and structure make it a valuable subject for scientific investigation, potentially leading to the discovery of new uses and applications for this compound.
Used in Material Science:
PHENOTHIAZINE-5-OXIDE may also find applications in material science, where its unique properties can be harnessed to develop new materials with specific characteristics. Its potential use in this field could lead to advancements in various industries, such as electronics, textiles, and coatings, among others.
Check Digit Verification of cas no
The CAS Registry Mumber 1207-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1207-71:
(6*1)+(5*2)+(4*0)+(3*7)+(2*7)+(1*1)=52
52 % 10 = 2
So 1207-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NOS/c14-15-11-7-3-1-5-9(11)13-10-6-2-4-8-12(10)15/h1-8,13H
1207-71-2Relevant articles and documents
Ozonization of phenothiazine and its analogues
Matsui,Miyamoto,Shibata,Takase
, p. 2526 - 2530 (1984)
When phenothiazine and phenoxazine were ozonized in dichloromethane, the cation radicals and the ozonate anion radicals were detected, whereas, in the ozonization of phenoxathiin and thianthrene, these radicals were not observed. Formation of these radicals was more favorable as greater was the polarity of the solvent and lower was the oxidation potential of the substrate. Ozonization of phenothiazine and phenoxazine in polar solvents was explained by the electron-transfer mechanism accompanied by the electrophilic ozone attack, and that of phenoxathiin and thianthrene by the electrophilic ozone attack alone.
Metal substitution in thermolysin: Catalytic properties of tungstate thermolysin in sulfoxidation with H2O2
Bakker, Martin,Van Rantwijk, Fred,Sheldon, Roger A.
, p. 622 - 625 (2007/10/03)
The catalytic Zn2+ ion was extracted from thermolysin, which had been covalently bound to Eupergit C. The apo-enzyme incorporated the oxometallate anions MoO42-, SeO42-, and WO42- with partial restoration of the proteolytic activity. Tungstate thermolysin was moderately active in the sulfoxidation of thioanisole by hydrogen peroxide, whereas its activity towards phenylmercaptoacetophenone, which was designed to bind well in the active site of thermolysin, was much higher.
