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1-Hexanone, 2-methyl-1-(2-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139984-00-2

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139984-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139984-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,9,8 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139984-00:
(8*1)+(7*3)+(6*9)+(5*9)+(4*8)+(3*4)+(2*0)+(1*0)=172
172 % 10 = 2
So 139984-00-2 is a valid CAS Registry Number.

139984-00-2SDS

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 2-methyl-1-pyridin-2-ylhexan-1-one

1.2 Other means of identification

Product number -
Other names 1-Hexanone,2-methyl-1-(2-pyridinyl)

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:139984-00-2 SDS

139984-00-2Downstream Products

139984-00-2Relevant academic research and scientific papers

Synthesis, characterisation and reactivity of rare 46-electron tri-ruthenium clusters

Ellul, Charles E.,Lowe, John P.,Mahon, Mary F.,Raithby, Paul R.,Whittlesey, Michael K.

, p. 4518 - 4523 (2018)

[Ru3(CO)12] reacts at room temperature with N-alkyl substituted 6-membered ring N-heterocyclic carbenes (6-NHC) to form [Ru3(6-NHC)(CO)10] (6-NHC = 6-iPr 1, 6-Et 2 and 6-Me 4), rare examples of coordinatively unsaturated (46-electron) ruthenium clusters. Complexes 1, 2 and 4 have been structurally characterised, along with the tetranuclear ruthenium cluster [Ru4(6-Et)2(CO)11] 3 that is formed along with 2. The degradation of the 6-iPr derivative 1 by pyrimidinium salt elimination helped to explain the poor activity of the complex in the catalytic acylation of pyridine.

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