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2-Propen-1-amine, N,N-diethyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13044-40-1

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13044-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13044-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13044-40:
(7*1)+(6*3)+(5*0)+(4*4)+(3*4)+(2*4)+(1*0)=61
61 % 10 = 1
So 13044-40-1 is a valid CAS Registry Number.

13044-40-1Upstream product

13044-40-1Downstream Products

13044-40-1Relevant academic research and scientific papers

Organomagnesium Inner Complexes, Part I. Bis(dialkylaminoalkyl)- and Bis(alkoxybutyl)magnesium Compounds

Angermund, Klaus,Bogdanovic, Borislav,Koppetsch, Gudrun,Krueger, Carl,Mynott, Richard,et al.

, p. 455 - 466 (2007/10/02)

A series of magnesium inner complexes has been prepared by reacting MgH2 (prepared by homogeneous catalysis) with dialkylallyl- and -3-butenylamines and -3-butenylethers in the presence of catalytic amounts of ZrCl4.The monomeric nature of bis(4-methoxybutyl)magnesium has been confirmed by X-ray diffraction.The analogous syntheses of bis(3-alkoxypropyl)magnesium compounds failed: cleavage of the allyl ether with elimination of propene occurred.This cleavage reaction is accelerated by catalytic amounts of NiCl2 or ZrCl4. - Keywords: Magnesium, Inner Complexes, Crystal Structure, X-Ray

Chemical Reactivities of Coordinatively Unsaturated Hydridotris(phosphonite)cobalt(I) Species Photogenerated towards Allylic and Related Compounds

Onishi, Masayoshi,Oishi, Shigero,Sakaguchi, Mitoshi,Takaki, Isato,Hiraki, Katsuma

, p. 3925 - 3930 (2007/10/02)

Pyrex-filtered photoirradiation with a high-pressure Hg lamp was performed for a thermally inert hydridocobalt(I) CoH4 in the presence of some allylic compounds.Allyl benzoate and allyl phenyl ether showed the cleavage of allylic-O bonds to give propene in a stoichiometric quantity to the complex charged.Photoassisted catalytic double-bond migration occured for N-allylacetamide, N,N-diethylallylamine, and allylbenzene to afford the respective (E)- and (Z)-1-propenyl derivatives with kinetically controlled, E, Z compositions, and the fractions of Z isomers at the initial stage of the reaction proceeding were near 79, 30, and 20percent, respectively.Laser flash photolysis study revealed that the double-bond migration was initiated by the coordination of the substrates through C=C double bond rather than nitrogen or oxygen donor-atom to the coordinatively unsaturated species "CoH3" photogenerated.

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