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Diethyl (dimethylamino)phenylmethylidenemalonate is a complex organic compound with the chemical formula C19H23NO4. It is a derivative of malonic acid, featuring a phenyl ring with a dimethylamino group attached to the phenylmethylidene moiety. diethyl (dimethylamino)phenylmethylidenemalonate is characterized by its conjugated double bond system and the presence of an amide group, which contributes to its chemical reactivity and potential applications in the synthesis of various pharmaceuticals and other organic compounds. Its structure allows for the exploration of different chemical reactions, such as nucleophilic addition, electrophilic substitution, and rearrangements, making it a valuable intermediate in organic chemistry.

4769-44-2

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4769-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4769-44-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,6 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4769-44:
(6*4)+(5*7)+(4*6)+(3*9)+(2*4)+(1*4)=122
122 % 10 = 2
So 4769-44-2 is a valid CAS Registry Number.

4769-44-2Downstream Products

4769-44-2Relevant academic research and scientific papers

(Z), Not (E) – An End to a Century of Confusion about the Double-Bond Stereoisomers of 3-Amino-2-cyanoacrylates

Donau, S?ren S.,Bechmann, Matthias,Müller, Norbert,Nielsen, Thorbj?rn T.,Wimmer, Reinhard

, p. 6408 - 6412 (2017)

Potent and selective myosin inhibitors are of vast scientific interest in the development of treatments for diseases involving myosin dysfunction or overactivity. A novel fungicide, ethyl 2-cyano-3-amino-3-phenylacrylate (commercialized as “phenamacril”), was recently identified as an inhibitor of myosin-5 in F. graminearum. Although the compound has been known since 1900, a general confusion concerning the stereochemical configuration at the exocyclic double bond persists in the literature, thus restricting further drug development of this compound and derivatives. By using NMR and quantum mechanical calculations, this work establishes the stereoconfiguration as the (Z) form and that the effect of a single hydrogen bond is crucial in keeping these types of molecules in a single configuration.

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