28950-34-7 Usage
Description
1,5,3,7-tetrathia-2,4,6,8-tetrazacycloocta-1,4,5,8-tetraene, also known as Tetrathia-2,4,6,8-tetrazacycloocta-1,4,5,8-tetraene, is a heterocyclic chemical compound with the chemical formula C4H4N4S4. It features an eight-membered ring containing four nitrogen and four sulfur atoms. 1$l^4,3,5$l^4,7-tetrathia-2,4,6,8-tetrazacycloocta-1,4,5,8-tetraene is known for its unique structure and properties, making it a promising candidate for applications in coordination chemistry and materials science.
Uses
Used in Coordination Chemistry:
1,5,3,7-tetrathia-2,4,6,8-tetrazacycloocta-1,4,5,8-tetraene is used as a ligand in coordination chemistry for the formation of metal complex compounds. Its unique structure allows it to chelate with metal ions, forming stable complexes with potential applications in various fields.
Used in Materials Science:
In materials science, 1,5,3,7-tetrathia-2,4,6,8-tetrazacycloocta-1,4,5,8-tetraene is utilized for its potential to contribute to the development of new materials with unique properties. Its heterocyclic nature and reactivity make it a candidate for use in the synthesis of advanced materials with specific characteristics.
Used in Chemical Reactions and Catalysis:
Due to its high reactivity, 1,5,3,7-tetrathia-2,4,6,8-tetrazacycloocta-1,4,5,8-tetraene is employed in various chemical reactions and catalysis processes. Its ability to participate in different types of reactions allows it to be a versatile component in the synthesis of various compounds and the development of catalytic systems.
Check Digit Verification of cas no
The CAS Registry Mumber 28950-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28950-34:
(7*2)+(6*8)+(5*9)+(4*5)+(3*0)+(2*3)+(1*4)=137
137 % 10 = 7
So 28950-34-7 is a valid CAS Registry Number.
InChI:InChI=1/N4S4/c1-5-2-7-4-8-3-6-1
28950-34-7Relevant articles and documents
Burt, F. P.
, p. 1171 - 1174 (1910)
Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+
Makarov, Alexander Yu.,Bagryanskaya, Irina Yu.,Zhivonitko, Vladimir V.
, p. 968 - 972 (2020/08/26)
[Figure not available: see fulltext.] Reactions of 1,3λ4δ2,2,4-benzothiadiazines with SCl2, C6F5SCl, and [NS2][SbF6] leading to 1,2,3-benzodithiazolium salts (Herz salts) were in
The Pyrolysis of Heptathiazocine
Kudo, Yoshiyuki,Hamada, Shuichi
, p. 2391 - 2394 (2007/10/02)
Heptathiazocine was pyrolyzed into ammonia, tetrasulfur tetranitride, and tetrasulfur dinitride above 383 K in an argon atmosphere; then, the latter two intermediates finally degraded into sulfur and nitrogen.According to the stoichiometric correlation am
Vaporization of (SN)x: He I Photoelectron Spectrum and ab Initio Calculations for the S3N3 Radical
Lau, W. M.,Westwood, N. P. C.,Palmer, M. H.
, p. 3229 - 3237 (2007/10/02)
The S3N3 radical, never previously characterized, is shown to be the major semistable component of the vaporization products of the (SN)x polymer, as identified by He I photoelectron spectroscopy and in situ quadrupole mass spectrometry.This species can be recondensed to yield the (SN)x polymer and other colored materials.Revaporization produces S3N3 in addition to S4N4, S4N2, and S2N2.Ab initio calculations with better than a double-ζ basis set and including configuration interaction provide evidence for a 2A2 radical with a planar ring geometry close to D3h.The ground-state cation also has a planar ring geometry with 3A2' favored over 1A1'.