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2-Butynedioic acid bis(triphenylstannyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73940-87-1

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73940-87-1 Usage

Hazard

A poison.

Check Digit Verification of cas no

The CAS Registry Mumber 73940-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,4 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73940-87:
(7*7)+(6*3)+(5*9)+(4*4)+(3*0)+(2*8)+(1*7)=151
151 % 10 = 1
So 73940-87-1 is a valid CAS Registry Number.
InChI:InChI=1/6C6H5.C4H2O4.2Sn/c6*1-2-4-6-5-3-1;5-3(6)1-2-4(7)8;;/h6*1-5H;(H,5,6)(H,7,8);;/r2C18H15Sn.C4H2O4/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;5-3(6)1-2-4(7)8/h2*1-15H;(H,5,6)(H,7,8)

73940-87-1SDS

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 bis(triphenylstannyl) but-2-ynedioate

1.2 Other means of identification

Product number -
Other names -

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:73940-87-1 SDS

73940-87-1Downstream Products

73940-87-1Relevant academic research and scientific papers

Preparation and structure of triorganotin, triorganolead and tetraphenylantimony derivatives of acetylenedicarboxylic acid, terephthalic acid and dithioterephtalic acid

Glowacki, A.,Huber, F.,Preut, H.

, p. 278 - 285 (2007/10/02)

Triorganotin, triorganolead and tetraphenylantimony derivatives of acetylenedicarboxylic acid (H2ADC), terephthalic acid (H2TER) and dithioterephthalic acid (H2DTT) (R3M)2X (M= Sn, Pb; R= Me, Ph; X= ADC, TER, DTT) and (Ph4SB)2X (X= ADC, TER) were prepared by neutralization of R3MOH or PH4SbOH with the appropriate acid (X= ADC, DTT) or by reaction of R3MCl or Ph4SbCl with K2TER.The crystal structures of (Me3Sn)2ADC and (Me3Sn)2TER were determined by X-ray diffraction.The Sn atoms are slightly distorted trigonal-bipyramidal environments, with C(Me) in the equatorial plane and O(carboxyl) in apical positions.The carboxylate groups are bridging, leading to the formation of two-dimensional polymer of puckered 22-membered and 26-memberd rings.From vibrational spectra, analogous structures are inferred for solid (Ph3Sn)2ADC, (R3Pb)2ADC (R= Me, Ph), and (Me3Pb)2TER, but structures with unidentate -COO and -COS groups and tetracoordinated Sn or Pb and pentacoordinated Sb are proposed for the other compounds.The DTT ligands are linked by S bonds to M.According to IR and 1H NMR studies the polymeric species dissociate on dissolution so that generally species with unidentate carboxylate groups are present.Sn and Pb in (R3M)2X (X= ADC, TER) are apparently tetracoordinated in CHCl3, but pentacoordinated in DMSO by addition of a solvent molecule.

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