943768-51-2 Usage
Uses
Used in Pharmaceutical Research:
(E)-4-(5-Bromo-2-methoxy-phenyl)-but-3-en-2-one is used as a pharmaceutical compound for its potential applications in the treatment of various diseases. Its unique structure and reactivity contribute to its potential as a therapeutic agent.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-4-(5-Bromo-2-methoxy-phenyl)-but-3-en-2-one is used as a building block for the synthesis of complex organic molecules. Its alpha, beta-unsaturated ketone structure provides unique reactivity, facilitating the creation of new compounds with diverse applications.
Used in Chemical Reactions:
(E)-4-(5-Bromo-2-methoxy-phenyl)-but-3-en-2-one is also used as a reactant in chemical reactions due to its distinctive alpha, beta-unsaturated ketone structure. This feature allows for versatile applications in the development of new chemical entities with potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 943768-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,7,6 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 943768-51:
(8*9)+(7*4)+(6*3)+(5*7)+(4*6)+(3*8)+(2*5)+(1*1)=212
212 % 10 = 2
So 943768-51-2 is a valid CAS Registry Number.
943768-51-2Relevant academic research and scientific papers
Silva, Ana L.,Quiroz, Beatriz,Maldonado, Luis A.
, p. 2055 - 2058 (1998)
Good yields of aldols, formed by reaction of the solvent acetone with some selected phenolic aldehydes, were obtained under Williamson arylmethyl ether conditions (Me2SO4 and K2CO3 in acetone).
Gallium(III) chloride catalyzed stereoselective synthesis of E-configured α,β-unsaturated ketones
Yadav,Reddy, B. V. Subba,Gupta, Manoj K.,Dash, Uttam,Pandey, Sushil K.
, p. 809 - 811 (2007/12/26)
A simple and highly stereoselective method has been developed for the synthesis of E-configured α,β-unsaturated ketones using gallium(III) chloride as a novel catalyst. This new procedure offers significant advantages such as high conversions, short reac-tion times and enhanced E-selectivity together with mild reaction conditions. Georg Thieme Verlag Stuttgart.
