59586-13-9 Usage
Uses
Used in Plastics Industry:
3-(TRICHLOROSTANNYL)METHYLPROPANOATE is used as a stabilizer in the production of PVC plastics for its ability to prevent the degradation of the polymer, thereby enhancing the durability and longevity of the final product. 3-(TRICHLOROSTANNYL)METHYLPROPANOATE's stabilizing properties are crucial in maintaining the structural integrity and performance of PVC materials in various applications, including construction, automotive, and packaging industries.
However, due to the potential environmental and health risks associated with 3-(TRICHLOROSTANNYL)METHYLPROPANOATE, there is a growing interest in developing alternative stabilizers that can offer similar benefits without the associated hazards. This has led to ongoing research and development efforts aimed at finding safer and more sustainable solutions for PVC stabilization.
Check Digit Verification of cas no
The CAS Registry Mumber 59586-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,8 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59586-13:
(7*5)+(6*9)+(5*5)+(4*8)+(3*6)+(2*1)+(1*3)=169
169 % 10 = 9
So 59586-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H7O2.3ClH.Sn/c1-3-4(5)6-2;;;;/h1,3H2,2H3;3*1H;/q;;;;+3/p-3/rC4H7Cl3O2Sn/c1-9-4(8)2-3-10(5,6)7/h2-3H2,1H3
59586-13-9Relevant academic research and scientific papers
ALCOHOLYSIS OF (2-METHOXYCARBONYL)ETHYLTIN COMPOUNDS
Cheng, Hong-Shing,Hwang, Tsai-Lih,Liu, Chao-Shiuan
, p. 43 - 52 (2007/10/02)
Under acid or base catalysis, di(2-alkoxycarbonylethyl)tin dichlorides of various R groups, (ROCOCH2CH2)2SnCl2, can be prepared conveniently in high yield by alcoholysis of (CH3OCOCH2CH2)2SnCl2 in various alcohols, ROH (R=C2H5, C4H9, iso-C4H9, C5H11, C6H5
REDISTRIBUTION REACTIONS OF β-CARBOALKOXYETHYLTIN COMPOUNDS
Burley, Joseph W.,Hutton, Ronald E.
, p. 165 - 176 (2007/10/02)
Carboalkoxyethyltin compounds undergo redistribution reactions at faster rates than similar unsubstituted alkyltin compounds.In redistribution reactions between SnCl4 and carboalkoxyethyltin compounds stable intermolecular complexes are formed.Rate enhancement is explained in terms of intra- and intermolecular coordination effects.Where strong intermolecular coordination effects are observed, specific electrophilic cleavage of the carboalkoxyethyl group can occur in preference to alkyl cleavage in mixed carboalkoxyethylalkyltin compounds.The presence of a β-ester function can catalyse both alkyl/chlorine and alkyl/alkyl' exchange reactions.
