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61244-93-7

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61244-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61244-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,4 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61244-93:
(7*6)+(6*1)+(5*2)+(4*4)+(3*4)+(2*9)+(1*3)=107
107 % 10 = 7
So 61244-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H2O/c1-2-3-4/h1H2

61244-93-7SDS

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 propa-1,2-dien-1-one

1.2 Other means of identification

Product number -
Other names Propadien-1-one

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:61244-93-7 SDS

61244-93-7Downstream Products

61244-93-7Relevant academic research and scientific papers

IR SPECTRAL STUDY AND SEMIEMPIRICAL CALCULATIONS OF THE THERMAL DECOMPOSITION PATHWAYS OF SOME SUBSTITUTED FURANDIONES

Aycard, Jean-Pierre,Bodot, Hubert,Hillebrand, Mihaela,N'Guessan, Thomas Y.,Hnach, Mochamed,et al.

, p. 686 - 695 (2007/10/02)

Furan-2,3-diones, structurally related to ascorbic acid, show potential antitumour physiological activity.Previous studies on this class of compounds have been devoted to their reactivity and thermal decomposition in solutions.It was reported, that 5-(p-R-phenyl)furan-2,3-dione with R=H, CH3, Cl, Br undergoes thermal decomposition in benzene and methyl alcohol solutions with elimination of carbon monoxide, the reaction product being able to react further to afford stable products.On another side, previous studies on the photochemical decomposition of these compounds in an Ar matrix at 15 K, in a KBr matrix and in solution have demonstrated the elimination of carbon dioxide as being the first reaction step.The reaction intermediates, as evidenced by Fourier Transform IR spectrometry, are either a ketene and/or cyclopropenone.

Flash vacuum pyrolysis of 2-diazo-8-oxabicyclo[3.2.1]oct-6-en-3-ones. A new method for the preparation of propadienones

Brahms,Dailey

, p. 1381 - 1384 (2007/10/02)

When diazoketones 3a and 3b are pyrolysed at 430°C and 10-4 torr, they undergo loss of N2 followed by Wolff rearrangement and loss of furan by retro Diels-Alder reaction to yield the desired propadienones 1(a,b). If argon is added to the pyrolysate mixture, these reactive compounds can be trapped under matrix isolation conditions at 22 K and observed by FTIR. Upon photolysis, 1b yields carbon monoxide and 2-butyne.

Ionized ethylidene ketene and its homologue methylene ketene

Terlouw, Johan K.,Holmes, John L.,Lossing, F. P.

, p. 1722 - 1724 (2007/10/02)

The gas phase pyrolyses of crotonic and acrylic-trifluoroacetic anhydrides were shown to yield ethylidene ketene and methylene ketene , respectively.The former was identified via the collisional activation mass spectrum of its molecular ion.The ionization energies of the two ketenes, 8.68 and 9.12 +/- 0.05 eV respectively, measured using energy selected electrons, lead to 215 and 233 kcal mol-1 for their ionic heats of formation.

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