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2-cyclohex-1-enyl-propionic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61346-65-4

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61346-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61346-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,4 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61346-65:
(7*6)+(6*1)+(5*3)+(4*4)+(3*6)+(2*6)+(1*5)=114
114 % 10 = 4
So 61346-65-4 is a valid CAS Registry Number.

61346-65-4Relevant academic research and scientific papers

Regio- and Stereoselectivity of Water Elimination as a Function of Ring Size

Greve, Bjoern,Imming, Peter

, p. 8058 - 8062 (1997)

The elimination of water from tertiary alcohols was studied for carbocycles of ring size 5-16. The resulting olefins 3-5 were discriminated by NMR spectroscopy. The relative amount of their formation reflects the steric idiosyncrasies of the respective ri

Effiziente Synthese neuer 2-Cycloalk(en)yl-propansaeure-Derivate - mittlere und grosse Ringe als Bioisostere von Alkylphenylresten?

Greve, Bjoern,Imming, Peter,Laufer, Stefan

, p. 1312 - 1314 (2007/10/03)

Stichworte: Cycloalkanone, Cyclooxygenase-Inhibitoren, Mittlere Ringe, Zinkverbindungen

An Efficient Entry Into Butenolides: Synthesis Of (+/-) Mintlactone

Chavan, Subhash P.,Zubaidha, P. K.,Ayyangar, Nagaraj R.

, p. 4605 - 4608 (2007/10/02)

Osmylation of β,γ-unsaturated esters and acid catalysed cyclisation of the resultant diols generate butenolides in high yields.

PHOTODECONJUGAISON ENANTIOSELECTIVE D'ESTERS ET DE LACTONES CONJUGUEES EN PRESENCE D'EPHEDRINE

Henin, Francoise,Mortezaei, Reza,Muzart, Jacques,Pete, Jean-Pierre,Piva, Oliverier

, p. 6171 - 6196 (2007/10/02)

α,β-unsaturated esters and α-alkylidene lactones bearing one γ-hydrogen on the unsaturated chain, were deconjugated by irradiation with UV light (λ=254 nm).When the reaction was carried out in the presence of (+) or (-) ephedrine, an enantioselective C-protonation of the photodienolic intermediate led to the deconjugated ester with an enantiomeric excess up to 30 percent.The scape of the reaction and the configuration of the new asymmetric center are discussed.

O-SILYLATED ENOLATES IN ORGANIC SYNTHESIS: SULPHUR-MEDIATED ALKYLATION OF ESTERS WITH ALKENES.

Patel, Shailesh K.,Paterson, Ian

, p. 1315 - 1318 (2007/10/02)

O-Silylated ester enolates can be alkylated, under ZnBr2-catalysis, by the PhSCl-adducts of mono- and di-substituted alkenes to give γ-phenylthioesters, from which sulphur can be removed both reductively and oxidatively.This alkene carbosulphenylation rea

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