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13703-97-4

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13703-97-4 Usage

General Description

2,4,6-tris-sulfanyl-1,3,5,2,4,6-trithiatriborinane is a chemical compound consisting of three boron atoms and six sulfur atoms. It is more commonly known as borotrithiadiene and has a cyclic structure. 2,4,6-tris-sulfanyl-1,3,5,2,4,6-trithiatriborinane is a sulfur analog of borane and has been studied for its potential use in organometallic chemistry and as a ligand in coordination chemistry. It has also been investigated for its potential use as a building block in the synthesis of other sulfur-containing compounds. Borotrithiadiene is a highly reactive compound and can react with various organic and inorganic compounds, making it a valuable reagent in organic synthesis. Its 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

13703-97-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(sulfanyl)-1,3,5,2,4,6-trithiatriborinane

1.2 Other means of identification

Product number -
Other names Borothiine-2,4,6-trithiol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13703-97-4 SDS

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.

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