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3047-10-7

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3047-10-7 Usage

General Description

HEXA(CYCLOHEXYL)DITIN is a chemical compound with the molecular formula C12H24Sn. It is a organotin compound that is used in various industrial applications such as in the production of plastics, rubber, and adhesives. This chemical is also used as a stabilizer in polyvinyl chloride (PVC) and can be found in some fungicides. However,

Check Digit Verification of cas no

The CAS Registry Mumber 3047-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3047-10:
(6*3)+(5*0)+(4*4)+(3*7)+(2*1)+(1*0)=57
57 % 10 = 7
So 3047-10-7 is a valid CAS Registry Number.
InChI:InChI=1/6C6H11.2Sn/c6*1-2-4-6-5-3-1;;/h6*1H,2-6H2;;/r2C18H33Sn/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h2*16-18H,1-15H2

3047-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name HEXA(CYCLOHEXYL)DITIN

1.2 Other means of identification

Product number -
Other names hexacyclohexylditin

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:3047-10-7 SDS

3047-10-7Relevant articles and documents

Synthesis and characterization of lipophilic organotins. Application to the functionalization of silica gel

Dumartin, Marie-Laurence,El Hamzaoui, Hicham,Jousseaume, Bernard,Rascle, Marie-Claude,Toupance, Thierry,Allouchi, Hassan

, p. 5576 - 5580 (2008/10/09)

The synthesis of the lipophilic docosyltri(hex-1-ynyl)tin was achieved in three steps according to two different synthetic pathways. This compound reacted with nonporous silica to yield surface-modified silica via the loss of the three alkynyl functionalities and the formation of Sibulk_O-Sn-C bonds. The reactivity and the maximum chain loading reached were compared to those obtained with the heptadecafluorodecyltin analogue. The differences observed were rationalized in terms of electronic demand and cross-sectional area of the grafted chain, as evidenced by FTIR spectroscopy and X-ray crystal structures of the precursors.

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