6265-24-3 Usage
Description
(E)-3-(4-methoxyphenyl)-N-methyl-prop-2-enamide is a chemical compound with the molecular formula C12H15NO2. It is a propenamide derivative characterized by the presence of a methyl group and a methoxyphenyl group attached to the carbon-carbon double bond. (E)-3-(4-methoxyphenyl)-N-methyl-prop-2-enamide is known for its potential biological activities and pharmacological properties, which make it a valuable component in the field of drug discovery and development. It is commonly used as a starting material in the synthesis of various pharmaceuticals and organic compounds. (E)-3-(4-methoxyphenyl)-N-methyl-prop-2-enamide should be handled and stored according to standard chemical safety practices and guidelines.
Uses
Used in Pharmaceutical Synthesis:
(E)-3-(4-methoxyphenyl)-N-methyl-prop-2-enamide is used as a starting material for the synthesis of various pharmaceuticals and organic compounds. Its unique structure and functional groups make it a versatile building block in the development of new drugs and molecules with potential therapeutic applications.
Used in Drug Discovery and Development:
Due to its potential biological activities and pharmacological properties, (E)-3-(4-methoxyphenyl)-N-methyl-prop-2-enamide is used as a valuable component in drug discovery and development. Researchers can leverage its chemical structure to design and create novel compounds with specific therapeutic targets, potentially leading to the development of new medications for various diseases and conditions.
Used in Chemical Research:
(E)-3-(4-methoxyphenyl)-N-methyl-prop-2-enamide is also utilized in chemical research to study the properties and reactivity of propenamide derivatives. This can contribute to a better understanding of the structure-activity relationships in this class of compounds and may lead to the discovery of new synthetic methods or applications in various chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6265-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6265-24:
(6*6)+(5*2)+(4*6)+(3*5)+(2*2)+(1*4)=93
93 % 10 = 3
So 6265-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO2/c1-12-11(13)8-5-9-3-6-10(14-2)7-4-9/h3-8H,1-2H3,(H,12,13)/b8-5+
6265-24-3Relevant articles and documents
Tandem superelectrophilic hydroarylation of CC bond and carbonyl reduction in cinnamides: Synthetic rout to 3,3-diarylpropylamines, valuable pharmaceuticals
Zakusilo, Dmitry N.,Ryabukhin, Dmitry S.,Boyarskaya, Irina A.,Yuzikhin, Oleg S.,Vasilyev, Aleksander V.
, p. 102 - 108 (2015/02/02)
Cinnamides ArCHCHCONRR′ in reactions with arenes Ar′H under the action of Bronsted (TfOH, FSO3H) or Lewis (AlBr3) superacids at rt for 1-2 h give CC bond hydroarylation products ArAr′CHCH2CONRR′ in yields of 63-98%. Reduction (LiAlH4/Et2O) of carbonyl group in the latter results in the formation of 3,3-diarylpropylamines ArAr′CHCH2CH2NRR′, valuable drugs. The reaction intermediates, superelectrophilic dications ArC+H-CH2C(OH+)NRR′, have been characterized by DFT calculations in terms of global electrophilicity index, natural charges, and atomic orbitals contributions.
