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Ethanone, 2-(hexahydro-2H-azepin-2-ylidene)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64944-51-0

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64944-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64944-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,4 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64944-51:
(7*6)+(6*4)+(5*9)+(4*4)+(3*4)+(2*5)+(1*1)=150
150 % 10 = 0
So 64944-51-0 is a valid CAS Registry Number.

64944-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(azepan-2-ylidene)-1-phenylethanone

1.2 Other means of identification

Product number -
Other names Ethanone,2-(hexahydro-2H-azepin-2-ylidene)-1-phenyl

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:64944-51-0 SDS

64944-51-0Relevant academic research and scientific papers

Gold-catalysed synthesis of exocyclic vinylogous amides and β-amino ketones: A detailed study on the 5-exo/6-endo-dig selectivity, methodology and scope

Scarpi, Dina,Begliomini, Stefano,Prandi, Cristina,Oppedisano, Alberto,Deagostino, Annamaria,G?mez-Bengoa, Enrique,Fiser, Béla,Occhiato, Ernesto G.

, p. 3251 - 3265 (2015/05/20)

The gold(I)-catalysed reaction of N-Boc-protected 6-alkynyl-3,4-dihydro-2H-pyridines, which gives synthetically useful vinylogous amides (β-enaminones), has been studied in detail, in order to optimize the reaction conditions, enlarge the scope and gain i

A new bicyclic oxazaborines with a bridged nitrogen atom, their thermic rearrangement and fluorescence properties

Josefík, Franti?ek,Svobodová, Markéta,Bertolasi, Valerio,?im?nek, Petr,MacHá?ek, Vladimír,Almonasy, Numan,?erno?ková, Eva

, p. 75 - 81 (2012/02/16)

Cyclic β-enaminones bearing secondary amino group react with 4-substituted benzenediazonium tetraphenylborates in dichloromethane to form substituted bicyclic [1,3,2λ4]oxazaborines The oxazaborines rearrange, on heating to 200 °C in the absence of solvent or in DMF or DMSO, to isomeric 2H-[1,2,4,3λ4]triazaborines. Previously prepared [1,3,2λ4]oxazaborines derived from acyclic β-enaminones bearing secondary amino group either did not undergo the rearrangement or with a lot of difficulties and with negligible yield. The fluorescence behaviour of the prepared triazaborines was observed. These compounds fluoresce in 2-methyltetrahydrofurane and in solid state under low temperatures.

Boric acid: a new regiospecific decarboxylating agent. Syntheses of cyclic imines, β-enaminones, and β-enaminodiketones from β-enaminoesters

Delbecq, Philippe,Bacos, Daniel,Celerier, Jean Pierre,Lhommet, Gerard

, p. 1201 - 1206 (2007/10/02)

The synthesis of cyclic imines 2, β-enaminones 6, and β-enaminodiketones 7 is described.Regio- and stereospecific thermolysis of β-enaminoesters 4 with boric acid permit these preparations in generally good yields. Key words: boric acid, cyclic β-enaminoesters, decarboxylation, cyclic imines, cyclic β-enaminones.

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