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Ruthenium, dichlorotetrakis(pyridine)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16997-43-6

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16997-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16997-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,9 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16997-43:
(7*1)+(6*6)+(5*9)+(4*9)+(3*7)+(2*4)+(1*3)=156
156 % 10 = 6
So 16997-43-6 is a valid CAS Registry Number.

16997-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-RuCl2(py)4

1.2 Other means of identification

Product number -
Other names trans-RuCl2(pyridine)4

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:16997-43-6 SDS

16997-43-6Upstream product

16997-43-6Relevant academic research and scientific papers

Donor-induced decomposition of the Grubbs catalysts: An intercepted intermediate

Lummiss, Justin A. M.,McClennan, William L.,McDonald, Robert,Fogg, Deryn E.

, p. 6738 - 6741 (2014)

The σ-alkyl species RuCl2(CH2PCy3)(py)3 (3a) is intercepted on adding pyridine to the first-generation Grubbs catalyst 1a during RCM or to the isolated resting-state species RuCl2(PCy3)2(=CH2) (2a). Complex 3a is formed by pyridine-induced displacement of PCy3 and nucleophilic attack of the liberated PCy3 on the methylidene carbon. The rapid, near-quantitative conversion of 2a into 3a indicates that nucleophilic attack by PCy3 is the primary deactivating event. Once formed, 3a decomposes more slowly via several competing pathways. One such pathway involves elimination of the σ-alkyl ligand as [CH3PCy3]Cl (A), following proton and chloride abstraction. Observation of nearly 80% 3a during RCM by 1a in the presence of pyridine confirms the relevance of this behavior to metathesis and implicates the resting-state methylidene 2a as the vulnerable species, rather than the metallacyclobutane intermediate. Any donor capable of displacing PCy3 and stabilizing a five-coordinate methylidene adduct is predicted to trigger the same deactivation sequence, steric factors permitting.

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