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12628-74-9

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12628-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 12628-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,6,2 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 12628-74:
(7*1)+(6*2)+(5*6)+(4*2)+(3*8)+(2*7)+(1*4)=99
99 % 10 = 9
So 12628-74-9 is a valid CAS Registry Number.

12628-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name palladium,triphenylphosphane

1.2 Other means of identification

Product number -
Other names PALLADIUM, (TRIPHENYLPHOSPHINE)-

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:12628-74-9 SDS

12628-74-9Relevant articles and documents

Activation and transformation of white phosphorus by palladium(ii) complexes

Kagirov,Voloshin,Rizvanov, I. Kh.,Sinyashin,Yakhvarov

, p. 1116 - 1118 (2010)

A reaction of bis(triphenylphosphine)palladium dibromide with white phosphorus in the presence of NaBPh4 selectively gives phosphorous acid H3PO3. The mechanism of the formation involves coordination of a white phosphorus molecule, ligand exchange, and hydrolysis of the coordinated P4 molecule in the coordination sphere of palladium.

Synthesis, Characterization, and Thermolytic Behaviour of η3-Allyl(methyl)(tertiary phosphine)palladium(II), and X-Ray Structure of the Cluster 2(μ-Cl)2(μ-dppm)2>*4C4H8O (dppm = Ph2PCH2PPh2)

Hayashi, Yoshihito,Matsumoto, Keiji,Nakamura, Yukio,Isobe, Kiyoshi

, p. 1519 - 1526 (2007/10/02)

Complexes of the type 3-allyl)Me(L)> 3, PPh3, PPh2Me, PPhMe2, or PBun3> have been synthesized and characterized by 1H, 13C n.m.r. and mass spectroscopy.The 3-C3H5)Me(L)> complexes thermally decompose with preferential evolution of ethane rather than but-1-ene, the allylic alkylation product.The participation of the binuclear methyl-bridged intermediate 3-allyl)2(μ-Me)2> (3) is supposed.Indirect support for this is given by the thermolysis of a toluene solution of (3).The effects of phosphines, alkenes, and other additives on the thermolysis products are discussed.The structure of a complex isolated from the 3-allyl)2(μ-Cl)2>-LiMe-Ph2PCH2PPh2 (dppm) reaction system in tetrahydrofuran was revealed by X-ray analysis as two μ-chloro-μ-allyl-dipalladium(I) units bridged by two dppm ligands.

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