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(1R,2R)-2-Methyl-2-vinyl-cyclopropanecarboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14027-57-7

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14027-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14027-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,2 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14027-57:
(7*1)+(6*4)+(5*0)+(4*2)+(3*7)+(2*5)+(1*7)=77
77 % 10 = 7
So 14027-57-7 is a valid CAS Registry Number.

14027-57-7Downstream Products

14027-57-7Relevant academic research and scientific papers

New catalytic system Cu(OAc)2-2,4-lutidine-ZnCl2 for olefin cyclopropanation with methyl diazoacetate

Gareev,Sultanova,Biglova,Dokichev,Tomilov

, p. 1784 - 1786 (2008)

A new efficient catalytic system consisting of Cu(OAc)2, 2,4-lutidine, and ZnCl2 was found for the cyclopropanation of unsaturated compounds with methyl diazoacetate. In the case of conjugated dienes, the process occurs regioselectively at the most alkylated C=C bond.

Polymeric dicarbonyl ruthenium(I) acetate - An efficient catalyst for alkene cyclopropanation with diazoacetates

Maas,Werle,Alt,Mayer

, p. 881 - 888 (2007/10/02)

The polymeric complex [Ru2(CO)4(μ-OAc)2](n) is the first Ru(I) catalyst that efficiently catalyzes cyclopropanation of alkenes with diazoacetic esters. The related dinuclear catalyst Ru2(CO)4(μ-OAc)2(MeCN)2 shows a similar performance only for cyclopropanation of monosubstituted alkenes.

TRANSITION-METAL-CATALYSED REACTIONS OF DIAZOESTERS : SYNTHESIS OF CHRYSANTHEMIC AND PERMETHRIC ACID ESTERS BY CYCLOPROPANATION OF CONJUGATED DIENES

Demonceau, A.,Noels, A. F.,Anciaux, A. J.,Hubert, A. J.,Teyssie, P.

, p. 949 - 952 (2007/10/02)

Pyrethroid precursors (permethric and chrysanthemic acid esters) are efficiently synthesized by rhodium(II)-catalysed cyclopropanation of the properly substituted conjugated diene.Reaction selectivities depend on both the catalyst counter-ion and the diazoester alkoxy-group (carbene precursor) and are attributed to non-bonded interactions.

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