31430-86-1 Usage
Uses
Used in Chemical Synthesis:
[(tetrachlorophthaloyl)bis(oxy)]bis(tributylstannane) is used as a building block for the synthesis of various organic compounds and materials. Its strong covalent bonding ability and high stability make it a preferred choice in creating a diverse range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(tetrachlorophthaloyl)bis(oxy)]bis(tributylstannane) is used as an intermediate in the development of new drugs. Its unique chemical properties allow for the creation of novel molecular structures with potential therapeutic applications.
Used in Materials Science:
[(tetrachlorophthaloyl)bis(oxy)]bis(tributylstannane) is utilized as a component in the design and fabrication of advanced materials. Its stability and bonding capabilities contribute to the development of materials with enhanced properties for various applications.
Environmental Considerations:
Due to its potential toxicity and environmental impact, [(tetrachlorophthaloyl)bis(oxy)]bis(tributylstannane) is used with caution in industrial applications. Proper handling, storage, and disposal protocols are essential to minimize any adverse effects on the environment and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 31430-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,3 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31430-86:
(7*3)+(6*1)+(5*4)+(4*3)+(3*0)+(2*8)+(1*6)=81
81 % 10 = 1
So 31430-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H2Cl4O4.6C4H9.2Sn/c9-3-1(7(13)14)2(8(15)16)4(10)6(12)5(3)11;6*1-3-4-2;;/h(H,13,14)(H,15,16);6*1,3-4H2,2H3;;/r2C12H27Sn.C8H2Cl4O4/c2*1-4-7-10-13(11-8-5-2)12-9-6-3;9-3-1(7(13)14)2(8(15)16)4(10)6(12)5(3)11/h2*4-12H2,1-3H3;(H,13,14)(H,15,16)
31430-86-1Relevant academic research and scientific papers
Synthesis, characterization and biological activities of some new organotin(IV) derivatives: Crystal structure of [(Sn Ph3) (OOCC6H4OH)] and [(SnMe3)2 (OOC)2C6Cl4 (DMSO)2]
Khawar Rauf,Adeel Saeed,Imtiaz-ud-Din,Bolte,Badshah,Mirza
, p. 3043 - 3048 (2008/12/21)
Some new organotin(IV) carboxylates 1-3 of 2-hydroxybenzoic acid (LA) and 4-6 of 2,3,4,5-tetrachloro-6-(methoxycarbonyl) benzoic acid (LB) have been synthesized, respectively, by the esterification of triorganotin oxide/hydroxide with the corresponding acids in an appropriate mole ratios. Multinuclear NMR (1H, 13C and 119Sn), IR and X-ray crystallographic studies were carried out to elucidate their structures both in solution and in solid state. The X-ray crystallographic data for 3 was recollected at low temperature. The compound 4 was dissolved in DMSO and a new compound 4 · 2DMSO [(SnMe3)2(OOC)2C6Cl4(DMSO)2] was crystallized out. The structure shows that two Sn moieties are attached to the ligand (LB) through two carboxylic groups. The two molecules of DMSO are coordinated to each of the Sn atoms via oxygen atom to terminate the conventional polymeric chain of trimethyl carboxylates to a discrete molecule, having trigonal bipyramidal geometry around the Sn atoms. Some of the synthesized compounds exhibited significant antifungal activities and have a potential to be used as drugs.
