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2-Propen-1-one, 1-[4-(dimethylamino)phenyl]-3-(4-methoxyphenyl)-, also known as 1-(4-dimethylaminophenyl)-3-(4-methoxyphenyl)-2-propen-1-one, is a complex organic compound with the molecular formula C17H19NO2. It is a derivative of 2-propen-1-one, featuring a 4-dimethylaminophenyl group and a 4-methoxyphenyl group attached to the 1 and 3 positions, respectively. 2-Propen-1-one, 1-[4-(dimethylamino)phenyl]-3-(4-methoxyphenyl)- is characterized by its conjugated double bonds and the presence of an electron-donating dimethylamino group and an electron-withdrawing methoxy group, which can influence its chemical reactivity and properties. It is an example of a chalcone, a type of organic compound that is often found in nature and has potential applications in various fields, including pharmaceuticals and materials science.

1158-21-0

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1158-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1158-21-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1158-21:
(6*1)+(5*1)+(4*5)+(3*8)+(2*2)+(1*1)=60
60 % 10 = 0
So 1158-21-0 is a valid CAS Registry Number.

1158-21-0Relevant academic research and scientific papers

Synthesis and biological evaluation of some new pyrazoline substituted benzenesulfonylurea/thiourea derivatives as anti-hyperglycaemic agents and aldose reductase inhibitors

Ovais, Syed,Pushpalatha,Reddy, G. Bhanuprakash,Rathore, Pooja,Bashir, Rafia,Yaseen, Shafiya,Dheyaa, Alhamza,Yaseen, Raed,Tanwar, Omprakash,Akthar, Mymoona,Samim, Mohammed,Javed, Kalim

, p. 209 - 217 (2014)

Seventeen new pyrazoline substituted benzenesulfonylurea/thiourea derivatives (2a-q) were synthesized and characterized by elemental analysis and various spectroscopic techniques viz; IR, 1H NMR, 13C NMR, and MS data. Thirteen compounds showed moderate to good anti-hyperglycaemic activity in glucose fed hyperglycaemic normal rats at the dose of 0.05 mM/kg b.w. On the basis of docking results nine compounds (2a, 2c, 2e, 2h, 2k, 2l, 2n, 2o and 2q) were evaluated for their ability to inhibit rat lens aldose reductase. Out of these six compounds (2h, 2k, 2l, 2n, 2o and 2q) were found more effective than the known ARI sorbinil. Five compounds (2h, 2k, 2l, 2n and 2o) showed significant dual action (anti-hyperglycaemic and aldose reductase inhibition).

Design and synthesis of novel pyridopyrimidine derivatives with anchoring non-coplanar aromatic extensions of EGFR inhibitory activity

Eissa, Amal A.M.,Aljamal, Kholoud F.M.,Ibrahim, Hany S.,Abdelrasheed Allam, Heba

, (2021/09/06)

The present study describes the synthesis of three series of 4-substituted pyridopyrimidin derivatives 4a-h, 5a-d. 6a-d, starting from 2-amino-6-(4-methoxyphenyl)-4-(4-(substituted) phenyl)nicotinonitrile 2a-d via the reaction with N,N-dimethyl-N-' substi

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