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methyl 3-ethyl-4,5-dihydroisoxazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55134-84-4

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55134-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55134-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,3 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55134-84:
(7*5)+(6*5)+(5*1)+(4*3)+(3*4)+(2*8)+(1*4)=114
114 % 10 = 4
So 55134-84-4 is a valid CAS Registry Number.

55134-84-4Downstream Products

55134-84-4Relevant academic research and scientific papers

Synthesis of 4,5-dihydroisoxazoles by condensation of primary nitro compounds with alkenes by using a copper/base catalytic system

Cecchi, Luca,De Sarlo, Francesco,Machetti, Fabrizio

experimental part, p. 7903 - 7912 (2009/09/06)

A new procedure for the synthesis of 4.5-dihydroisoxazoles by condensation of primary nitro compounds with olefins by using a copper/base catalytic system is described. The catalytic effect of copper(II) salts is evidenced by comparison of the reaction ra

4,5-Dihydroisoxazoles by copper(II)-catalysed condensation of primary nitroalkanes with dipolarophiles

Cecchi, Luca,De Sarlo, Francesco,Machetti, Fabrizio

, p. 2451 - 2453 (2008/03/28)

Primary aliphatic nitro compounds condense with substituted alkenes to give 4,5-dihydroisoxazoles under copper(II) acetate catalysis in the presence of tertiary amines. Apparently nitrile oxides are not intermediates, as no furoxans are detected in these

Synthesis of some isoxazolines and evaluation of carbon-13 NMR substituent parameters for 5-methyl substitution

Nagarajan, A.,Pillay, M. Krishna

, p. 938 - 941 (2007/10/02)

Some isoxazolines substituted at C-5 with phenyl and methoxycarbonyl groups have been synthesised and characterised.Carbon-13 NMR methyl substituent parameters for methyl substitution at C-5 carbon in these compounds have been evaluated.

A Convinient Preparative Method of Nitrile Oxides by the Dehydration of Primary Nitro Compounds with Ethyl Chloroformate or Benzenesulfonyl Chloride in the Presence of Triethylamine

Shimizu, Tomio,Hayashi, Yoshiyuki,Shibafuchi, Hiroshi,Teramura, Kazuhiro

, p. 2827 - 2832 (2007/10/02)

Three nitrile oxides (MeOCOCN->O, PhCN->O, and EtCN->O) were effectively generated in situ by dehydration of the corresponding primary nitro compounds (RCH2NO2) with PhSO2Cl or ClCOOEt in the presence of triethylamine.Various cycloadducts were prepared by the reaction of them with dipolarophiles.Some advantages of these methods are described in comparison with other known methods.

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