13703-97-4 Usage
Chemical composition
Consists of three boron atoms and six sulfur atoms.
Structure
Has a cyclic structure.
Analog
Sulfur analog of borane.
Potential uses
Studied for its potential use in organometallic chemistry, as a ligand in coordination chemistry, and as a building block in the synthesis of other sulfur-containing compounds.
Reactivity
Highly reactive compound that can react with various organic and inorganic compounds.
Value
Valuable reagent in organic synthesis.
Research interest
Unique structure and reactivity make it an interesting target for further research and potential applications in various fields of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 13703-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13703-97:
(7*1)+(6*3)+(5*7)+(4*0)+(3*3)+(2*9)+(1*7)=94
94 % 10 = 4
So 13703-97-4 is a valid CAS Registry Number.
InChI:InChI=1/B3H3S6/c4-1-7-2(5)9-3(6)8-1/h4-6H
13703-97-4Relevant articles and documents
Greene, F. T.,Margrave, J. L.
, p. 5555 - 5556 (1959)
Electronic Structure and Bonding in Cyclic B-S and B-Se Compounds Studied by Solid State 11B NMR
Conrady-Pigorsch, R.,Mueller-Warmuth, W.,Schwetlik, G.,Wienkenhoever, M.,Krebs, B.
, p. 453 - 458 (2007/10/02)
Solid state 11B (and in one case 10B) NMR spectra of four cyclic boron-chalcogen compounds have been measured at various frequencies and analysed in terms of nuclear quadrupole and chemical shift interactions.Application of the Townes-Dailey theory to the quadrupole results, corrected for ionic contributions to the electric field gradient and to the bonding, yields detailed information about the importance of ?-bonding in the respective materials.The occupation number of the 2pz orbitals of the sp2-hybridized boron atoms appear to be particularly large for systems containing chalcogen-chalcogen bridges.From both the chemical point of view and the spectroscopic result, among the six- and five-membered rings, diiodotriselenadiborolane is distinguished by an exceptional position.
