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butyl 3-(trichlorostannyl)propionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61470-34-6

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61470-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61470-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,7 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61470-34:
(7*6)+(6*1)+(5*4)+(4*7)+(3*0)+(2*3)+(1*4)=106
106 % 10 = 6
So 61470-34-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H13O2.3ClH.Sn/c1-3-5-6-9-7(8)4-2;;;;/h2-6H2,1H3;3*1H;/q;;;;+3/p-3/rC7H13Cl3O2Sn/c1-2-3-5-12-7(11)4-6-13(8,9)10/h2-6H2,1H3

61470-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl 3-trichlorostannylpropanoate

1.2 Other means of identification

Product number -
Other names 2-n-butoxycarbonylethyltin trichloride

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:61470-34-6 SDS

61470-34-6Downstream Products

61470-34-6Relevant academic research and scientific papers

The transesterification reaction of β-methoxycarbonylethyltin trichloride and its dimethylsulfoxide adduct with alcohols

Tian, Laijin,Zhou, Zhengyu,Zhao, Bin,Yu, Wentao,Yang, Ping

, p. 1363 - 1372 (2008/10/08)

The transesterification reaction of ss-methoxycarbonylethyltin trichloride and its dimethylsulfoxide adduct with alcohols is reported and the possible mechanism is suggested. A series of ss-alkoxycarbonylethyltin trichlorides and their dimethyl-sulfoxide adducts were synthesized and characterized by means of elemental analyses, IR and 1H NMR spectra and an X-ray single crystal diffraction study.

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.

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