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1-(4-bromophenyl)-3-(2,4,5-trimethoxyphenyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

941607-52-9

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941607-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 941607-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,6,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 941607-52:
(8*9)+(7*4)+(6*1)+(5*6)+(4*0)+(3*7)+(2*5)+(1*2)=169
169 % 10 = 9
So 941607-52-9 is a valid CAS Registry Number.

941607-52-9Downstream Products

941607-52-9Relevant academic research and scientific papers

An investigation on the key features of a D-π-A type novel chalcone derivative for opto-electronic applications

Shkir, Mohd.,Muhammad, Shabbir,AlFaify, Salem,Irfan, Ahmad,Patil, Parutagouda Shankaragouda,Arora, Manju,Algarni, Hamed,Jingping, Zhang

, p. 87320 - 87332 (2015)

The current study is focused on the donor-bridge-acceptor (D-π-A) type of novel organic charge transport and non-linear optical material, 1-(4-bromophenyl)-3-(2,4,5-trimethoxyphenyl) prop-2-en-1-one (2,4,5-TMBC) to spotlight its various important properti

Reinvestigation of structure-activity relationship of methoxylated chalcones as antimalarials: Synthesis and evaluation of 2,4,5-trimethoxy substituted patterns as lead candidates derived from abundantly available natural β-asarone

Kumar, Rakesh,Mohanakrishnan, Dinesh,Sharma, Abhishek,Kaushik, Naveen Kumar,Kalia, Kalpana,Sinha, Arun Kumar,Sahal, Dinkar

experimental part, p. 5292 - 5301 (2011/02/23)

We have examined the antimalarial structure-activity relationship of a series of methoxylated chalcones (A-CHCH-CO-B) against Plasmodium falciparum (3D7 strain) using fluorescence-based SYBR Green assay. Our study has revealed that electron releasing methoxy groups on ring A and electron withdrawing groups on ring B increases antimalarial potency while the positional interchange of these groups causes a decrease. In particular, 2,4,5-trimethoxy substitution pattern at ring A provided potent analogues which were easily derived from abundantly available natural β-asarone rich Acorus calamus oil. Cytotoxic evaluation indicated that the most active compounds 27 (IC50: 1.8 μM) and 26 (IC50: 2 μM) were also relatively non-toxic. Furthermore, compound 12 showed excellent resistance index of 1.1 against chloroquine resistant Dd2 strain of P. falciparum.

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