13817-04-4 Usage
Description
1-Oxa-2-thia(IV)-3-azaallene is a unique imide compound characterized by the presence of an imino group and an oxo group attached to an atom of sulfur. This distinctive molecular structure endows it with a range of potential applications across various industries.
Uses
Used in Pharmaceutical Industry:
1-Oxa-2-thia(IV)-3-azaallene is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved efficacy and selectivity, targeting a wide range of diseases and conditions.
Used in Chemical Synthesis:
In the field of chemical synthesis, 1-Oxa-2-thia(IV)-3-azaallene serves as a versatile building block for the creation of complex organic molecules. Its unique reactivity and functional groups enable the formation of a diverse array of compounds with potential applications in various industries, including materials science, agrochemicals, and specialty chemicals.
Used in Material Science:
1-Oxa-2-thia(IV)-3-azaallene is used as a component in the development of novel materials with enhanced properties. Its incorporation into polymers and other materials can lead to improved mechanical strength, thermal stability, and chemical resistance, making it valuable for applications in aerospace, automotive, and electronics industries.
Used in Agrochemicals:
In the agrochemical industry, 1-Oxa-2-thia(IV)-3-azaallene is used as a starting material for the synthesis of new pesticides and herbicides. Its unique structure allows for the development of more effective and environmentally friendly products, contributing to sustainable agriculture practices.
Used in Research and Development:
1-Oxa-2-thia(IV)-3-azaallene is also utilized in research and development efforts, where its unique properties and reactivity are explored for potential applications in various fields. This includes the development of new catalysts, sensors, and other advanced materials with specific functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 13817-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,1 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13817-04:
(7*1)+(6*3)+(5*8)+(4*1)+(3*7)+(2*0)+(1*4)=94
94 % 10 = 4
So 13817-04-4 is a valid CAS Registry Number.
InChI:InChI=1/HNOS/c1-3-2/h1H
13817-04-4Relevant articles and documents
Preparation, characterisation, quantum chemical calculations, and chemical reactions of sulfurdiimine, its silver and thallium salts as well as TlNSO
Haas, Alois,Fleischer, Ulrich,Maetschke, Matthias,Staemmler, Volker
, p. 681 - 692 (2008/10/08)
Reactions of (CH3)3SiNSNSi(CH3)3 with Ag[CF3C(O)O] or TlF respectively have allowed the formation of the highly explosive compounds M2[SN2] (M = Ag, Tl) in nearly quantitative yields. Under analogous conditions (CH3)3SiNSO and TlF formed non-explosive TlNSO again in about 100% yield. The reaction between (CH3)3SiNSNSi(CH3)3 and ICl was found to be easily reproducable and gave INSNI in good yields. INSNI was obtained also from K2[SN2] and ICl in 40% yield. The reaction of (CH3)3SiNSNSi(CH3)3 with CsF resulted in monosubstitution and the formation of CsNSNSi(CH3)3. INSNI reacted with HX (X = Cl, I) in closed systems to give S4N4, NH4X, IX and N2 as final products. Similar results were observed when M2[SN2] was treated with HX in Carius tubes. Besides higher yields of S4N4 small amounts of S4N3Cl and other not identified SN compounds were detected. In open systems HX reacted with M2[SN2] in dynamic vacuo explosively. Under matrix conditions preliminary tests showed that TlNSO formed with HX pure HNSO, characterised by a high quality matrix IR-spectrum. With the help of this metathetical reaction, the conditions for matrix-spectroscopic studies of the system MNSNM and HX could be optimized. If M2[SN2] was treated with HX analogously HNSNH was produced. The diimine was characterized by bands of comparable intensities, appearing in spectra of the products of the reaction which were assigned to the molecule. Identical bands were also observed when INSNI was treated with excess HX. If the procedure was carried out with 1:1 molar quantities, the formation of the primary produced HNSNI could be evidenced by IR-spectroscopy. Detailed quantum chemical ab inition calculations about structures, relative energies and vibrational spectra of the HNSNH-conformers as well as other possible SN2H2 isomeres were carried out. They confirmed the experimental results and assignments and strengthened the conclusion that HNSNH was present as a mixture of E,Z- and Z,Z-conformers.
