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E-2-(4-Chlorophenyl)-1-methyl-1-nitro-oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134964-66-2

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134964-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134964-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,6 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134964-66:
(8*1)+(7*3)+(6*4)+(5*9)+(4*6)+(3*4)+(2*6)+(1*6)=152
152 % 10 = 2
So 134964-66-2 is a valid CAS Registry Number.

134964-66-2Downstream Products

134964-66-2Relevant academic research and scientific papers

OXIDATIVE ADDITION OF HYDROXIDE ANIONS TO NITROALKENES VIA THE RADICAL ANIONS OF α-NITRO-OXIRANES

Bowman, W. Russel,Brown, David S.,Chaffin, Julie D. E.,Symons, Martyn C. R.,Jackson, Stuart W.,Willcocks, Neil A.

, p. 2285 - 2288 (1991)

Stereoselective oxidative addition of hydroxide anions to nitroalkenes was carried out using potassium ferricyanide to yield α-nitro-oxiranes by a novel non-chain mechanism involving cyclisation of alkoxide anions onto α-nitroalkyl radicals.

Regioselective Opening of Nitroepoxides with Unsymmetrical Diamines

Nosood, Yazdanbakhsh L.,Ziyaei Halimehjani, Azim,González, Florenci V.

, p. 1252 - 1258 (2018/02/09)

Nitroepoxides are easily transformed into benzodiazepines, tetrahydrobenzodiazepines, imidazopyridines, and N-alkyl tetrahydroquinoxalines by treatment with 2-aminobenzylamines, 2-aminopyridines, and N-alkyl 1,2-diaminobenzenes, respectively. Regioselectivity is controlled through attack of the most nucleophilic nitrogen of the unsymmetrical diamine to the β position of the epoxide. These reactions represent an efficient way to prepare privileged bioactive structures.

Preparation of Morpholines and Benzoxazines Starting from Nitroepoxides

Capel,Vidal-Albalat,Rodríguez,González

, p. 2572 - 2580 (2016/08/11)

Nitroepoxides are easily transformed into 2,3-disubstituted morpholines and 2,3-disubstituted benzoxazines in a two-step sequence by treatment with N-methylethanolamine and N-methyl-2-hydroxyaniline, respectively, in a highly stereoselective fashion.

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