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Manganese, decacarbonyl-m-1,4-phenylenedi- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17477-07-5

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17477-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17477-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,7 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17477-07:
(7*1)+(6*7)+(5*4)+(4*7)+(3*7)+(2*0)+(1*7)=125
125 % 10 = 5
So 17477-07-5 is a valid CAS Registry Number.

17477-07-5SDS

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 1,4-C6H3(Mn(CO)5)2

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:17477-07-5 SDS

17477-07-5Upstream product

17477-07-5Relevant academic research and scientific papers

Phenylene-bridged organometallic complexes of iron and manganese

Hunter, Allen D.,Szigety, Andrew B.

, p. 2670 - 2679 (2008/10/08)

The synthesis of the complexes 1,3-C6H4(MLn)2,1,4-C 6H4(MLn)2, and 1,3,5-C6H3(MLn)3 (where MLn = (η5-C5H5)Fe(CO)2, (η5-C5H4Me)Fe(CO)2, or Mn(CO)5) is described. These species are best prepared in two steps by metathesis of the organometallic anion, NaMLn, with the appropriate aroyl chloride to give acyl intermediates. These complexes were isolated and then thermally decarbonylated (in refluxing butyl ether and THF for the Fe and Mn complexes, respectively) to give the desired products in 40-90% overall yield. Their perfluoro analogues, 1,4-C6F4Fp?2 (where Fp? = (η5-C5H5)Fe(CO)2 or (η5-C5H4Me)Fe(CO)2), are prepared in 30-60% yield by the metathesis of 1,4-C6F4Li2 with Fp?I. These new materials have been fully characterized by conventional spectroscppic techniques and are shown to contain metal-arene σ bonds. Evidence is provided for partial dimetalloquinone character in the bonding of the para-substituted species. The reactions of the title compounds with phosphines (to give carbonyl substitution products) and with halogens (to give metal-aryl bond cleavage) are also reported.

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