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88652-66-8

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88652-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88652-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,5 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88652-66:
(7*8)+(6*8)+(5*6)+(4*5)+(3*2)+(2*6)+(1*6)=178
178 % 10 = 8
So 88652-66-8 is a valid CAS Registry Number.

88652-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [dibutyl-[hydroxy(phenyl)arsoryl]oxystannyl]oxy-phenylarsinic acid

1.2 Other means of identification

Product number -
Other names Stannane,dibutylbis[(hydroxyphenylarsinyl)oxy]

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:88652-66-8 SDS

88652-66-8Downstream Products

88652-66-8Relevant articles and documents

Oxy- and Thio-phosphorus Acid Derivatives of Tin. Part 12. A Moessbauer Spectroscopic Investigation of the Structures and Polymorphic Behaviour of Diorganotin(IV) Phenyl-phosphonates and -arsonates

Cunningham, Desmond,Firtear, Padraig,Molloy, Kiaran C.,Zuckerman, Jerald J.

, p. 1523 - 1528 (2007/10/02)

The phenylphosphonate and phenylarsonates Me2Sn, Me2Sn, and Bun2Sn are isolated as their α-modifications from the reaction of dimethyl- or di-n-butyl-tin dichloride with the monosodium salt of the appropriate acid. β-Modifications are obtained by removal of water from the monohydrates Me2Sn*H2O, Me2Sn*H2O, and Bun2Sn*H2O, obtained in turn from the reaction of the diorganotin dichloride with the disodium salt of the appropriate acid.Only one form of Ph2Sn was isolated; this can be obtained either from the direct reaction of diphenyltin dichloride with phenylphosphonic acid or by removal of water from Ph2Sn*H2O.On the basis of i.r. and variable-temperature Moessbauer spectroscopic and X-ray powder diffraction data it is suggested that the structures of the β-modifications and of Ph2Sn consist of infinite chains, and that chains with similar backbone structures occur in solid-state forms of their hydrate precursors.The α-modifications of Me2Sn and Bu(n)2Sn appear to have two-dimensional sheet structures in which tin achieves five-co-ordination, but the data do not preclude the possibility that α-Me2Sn has a more associated three-dimensional network structure, with tin in highly distorted octahedral sites.The complexes Me2Sn2, Bun2Sn2, and Bun2Sn2, obtained by the reaction of a diorganotin dihalide with the appropriate acid, have structures in which tin is in octahedral sites.It is suggested that these are chain structures in which chains are linked by strong hydrogen bonds.

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