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16182-63-1

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16182-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16182-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,8 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16182-63:
(7*1)+(6*6)+(5*1)+(4*8)+(3*2)+(2*6)+(1*3)=101
101 % 10 = 1
So 16182-63-1 is a valid CAS Registry Number.

16182-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dipotassium tetracarbonylferrate

1.2 Other means of identification

Product number -
Other names DIPOTASSIUM TETRACARBONYLFERRATE

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:16182-63-1 SDS

16182-63-1Relevant academic research and scientific papers

Synthesis and reactivity of [(R1R2N)2PH]Fe(CO)4 complexes. X-ray crystal structure of [(Ph2N)2PH]Fe(CO)4

Brunet, Jean-Jacques,Chauvin, Remi,Diallo, Ousmane,Donnadieu, Bruno,Jaffart, Jo?lle,Neibecker, Denis

, p. 390 - 395 (2007/10/03)

KHFe(CO)4 reacts with tris(amino)phosphines by substitution at phosphorus leading to [bis(amino)phosphine]tetracarbonyliron complexes [(R1R2N)2PH]Fe(CO)4. The X-ray structure has been determined for R1=R2=Ph. Deprotonation of these complexes with KH affords stable potassium phosphidotetracarbonylferrates which can be alkylated or acylated at phosphorus.

Ligand substitution processes on carbonylmetal derivatives. 1. Reaction of tetracarbonylhydridoferrates with phosphines

Brunet,Commenges,Kindela,Neibecker

, p. 1343 - 1350 (2008/10/08)

Ligand substitution processes on KHFe(CO)4 (1) have been demonstrated for the first time by reaction with various phosphines (2 equiv). The reaction times and the nature of the reaction products strongly depend on (i) the nature of the solvent, (ii) the cone angle of the phosphine, and (iii) the reaction conditions. In protic media (e.g. EtOH), phosphines with small cone angles (P(n-Bu)3, PMe2Ph) react with 1 below room temperature to give the newly characterized H2Fe(CO)2(PR3)2 in good yield, whereas phosphines with larger cone angles react only at higher temperature and afford the disubstituted Fe(CO)3(PR3)2 derivatives in quantitative yield. In aprotic medium (THF), phosphines (P(n-Bu)3, PPh3) react only slowly with 1 at room temperature but do so at reflux temperature to yield K2Fe(CO)4 (50%) and bis- or tris-(phosphine)carbonyliron derivatives. The reaction mechanism involves the formation of a monosubstituted K+[HFe(CO)3(PR3)]- derivative with a rate strongly dependent on the Tolman cone angle of the phosphine. In THF, this basic hydrido carbonyl anion reacts with 1 to yield K2Fe(CO)4 and H2Fe(CO)3(PR3). The latter further reacts to give bis- or tris(phosphine)carbonyliron derivatives. In ethanol, the monosubstituted K+[HFe(CO)3(PR3)]- derivative is protonated to give the neutral dihydride H2Fe(CO)3(PR3), which depending on the reaction conditions, is converted either to H2Fe(CO)2(PR3)2 by CO substitution (at low temperature) or to Fe(CO)3(PR3)2 by H2 elimination (at higher temperature). For phosphines exhibiting small cone angles, the disubstituted dihydride may react further with an excess of phosphine to yield the trisubstituted Fe(CO)2(PR3)3 derivative in good yield.

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