7512-67-6 Usage
Description
(2E)-1,2,3-triphenylprop-2-en-1-one, also known as chalcone, is a chemical compound with the molecular formula C22H16O. It is a yellow crystalline solid that is commonly used as a precursor in the synthesis of various organic compounds. Chalcone exhibits a wide range of biological activities, including anti-inflammatory, anti-cancer, and antioxidant properties. It is also used in the production of fluorescent dyes, as well as in the development of pharmaceutical drugs. Additionally, chalcone has been found to inhibit the growth of bacteria and fungi, making it a potential candidate for the development of antimicrobial agents. Overall, (2E)-1,2,3-triphenylprop-2-en-1-one is a versatile compound with various applications in the fields of chemistry, biology, and medicine.
Uses
Used in Pharmaceutical Industry:
(2E)-1,2,3-triphenylprop-2-en-1-one is used as a pharmaceutical precursor for the synthesis of various organic compounds. Its wide range of biological activities, such as anti-inflammatory, anti-cancer, and antioxidant properties, make it a promising candidate for the development of pharmaceutical drugs.
Used in Chemical Industry:
(2E)-1,2,3-triphenylprop-2-en-1-one is used as a chemical intermediate in the synthesis of various organic compounds. Its versatility as a precursor allows for the production of a wide range of chemical products.
Used in Biomedical Research:
(2E)-1,2,3-triphenylprop-2-en-1-one is used as a research tool in the study of biological activities and mechanisms. Its anti-inflammatory, anti-cancer, and antioxidant properties provide valuable insights into the development of new therapeutic agents.
Used in Antimicrobial Applications:
(2E)-1,2,3-triphenylprop-2-en-1-one is used as a potential antimicrobial agent due to its ability to inhibit the growth of bacteria and fungi. This makes it a candidate for the development of new antimicrobial drugs and treatments.
Used in Fluorescent Dye Production:
(2E)-1,2,3-triphenylprop-2-en-1-one is used in the production of fluorescent dyes. Its unique properties allow for the development of dyes with specific characteristics, making it useful in various applications such as imaging and sensing.
Check Digit Verification of cas no
The CAS Registry Mumber 7512-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7512-67:
(6*7)+(5*5)+(4*1)+(3*2)+(2*6)+(1*7)=96
96 % 10 = 6
So 7512-67-6 is a valid CAS Registry Number.
7512-67-6Relevant articles and documents
Method for synthesizing alpha, beta unsaturated ketone
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Paragraph 0016-0022, (2021/10/11)
The invention belongs to the technical field of chemical synthesis, and particularly relates to a method for synthesizing alpha, beta unsaturated ketone. The reaction adopts a synergetic catalysis system of Co(acac)2 or Co(acac)3, a ligand and AlMe3, provides a way for economically and selectively synthesizing alpha, beta unsaturated ketones by atoms, and has the advantages of high yield and wide substrate range.
Heterogeneous gold-catalyzed oxidative cross-coupling of propargylic acetates with arylboronic acids leading to (E)-α-arylenones
Liu, Dayi,Nie, Quan,Zhang, Rongli,Cai, Mingzhong
supporting information, p. 29 - 34 (2018/11/30)
An efficient heterogeneous gold-catalyzed oxidative cross-coupling of propargylic acetates with arylboronic acids has been developed that proceeds smoothly in the presence of Selectfluor and provides a general and powerful tool for the preparation of various valuable α-arylenones with moderate to good yields, excellent E-selectivity, and recyclability of the gold catalyst. The reaction is the first example of heterogeneous gold-catalyzed arylative rearrangement of propargylic acetates for construction of complex enones.
Palladium-catalyzed dehydrogenative β-arylation of simple saturated carbonyls by aryl halides
Gandeepan, Parthasarathy,Rajamalli,Cheng, Chien-Hong
, p. 4485 - 4489 (2015/01/09)
(Chemical Equation Presented) A versatile palladium-catalyzed synthesis of highly substituted α,β-unsaturated carbonyl compounds has been developed. In contrast to the known Heck-type coupling reaction of unsaturated carbonyl compounds with aryl halides, the present methodology allows the use of stable and readily available saturated carbonyl compounds as the alkene source. In addition, the reaction proceeds well with low catalyst loadings and does not require any expensive metal oxidants or ligands. A variety of saturated aldehydes, ketones, and esters are compatible for the reaction with aryl halides under the developed reaction conditions to afford α,β-unsaturated carbonyl compounds in good to excellent yields. A possible reaction mechanism involves a palladium-catalyzed dehydrogenation followed by Heck-type cross couplings.
