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α-Carbaethoxy-α-brom-β-phenyl-γ-nitro-buttersaeureaethylester is a complex organic chemical compound with the molecular formula C14H16BrNO6. It is a derivative of butyric acid, featuring an α-carbethoxy group, an α-bromine atom, a β-phenyl group, and a γ-nitro group. α-Carbaethoxy-α-brom-β-phenyl-γ-nitro-buttersaeureaethylester is characterized by its ester functional group, which is formed by the reaction of the carboxylic acid group with an alcohol. The presence of the nitro group and the bromine atom in the molecule contributes to its reactivity and potential applications in chemical synthesis. It is important to note that the compound's structure and properties make it a potentially hazardous substance, requiring careful handling and storage.

22985-40-6

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22985-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22985-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,8 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22985-40:
(7*2)+(6*2)+(5*9)+(4*8)+(3*5)+(2*4)+(1*0)=126
126 % 10 = 6
So 22985-40-6 is a valid CAS Registry Number.

22985-40-6Relevant academic research and scientific papers

Enantioselective synthesis of nitrocyclopropanes via conjugate addition of bromomalonate to nitroalkenes catalyzed by Ni(II) complexes

Lee, Hyun Joo,Kim, Sun Mi,Kim, Dae Young

experimental part, p. 3437 - 3439 (2012/08/08)

A novel one-pot methodology for the catalytic enantioselective synthesis of highly functionalized nitrocyclopropanes promoted by chiral nickel complexes is developed. The treatment of bromomalonates with nitroalkenes under the mild reaction conditions aff

Stereoselective synthesis of functionalised cyclopropanes from nitroalkenes via an organocatalysed Michael-initiated ring-closure approach

Russo, Alessio,Lattanzi, Alessandra

experimental part, p. 1155 - 1157 (2010/10/20)

Synthetically useful nitrocyclopropanes are easily obtained via Michael addition of dimethyl bromomalonate to nitrostyrenes promoted by commercially available (S)-α,α-di-β-naphthlyl-2-pyrrolidinemethanol as the catalyst, followed by DABCO-mediated intramo

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