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1-acetyl-5-(3,4-dimethoxyphenyl)-3-(3-nitrophenyl)-4,5-dihydro-(1H)-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1290604-86-2

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1290604-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1290604-86-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,6,0 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1290604-86:
(9*1)+(8*2)+(7*9)+(6*0)+(5*6)+(4*0)+(3*4)+(2*8)+(1*6)=152
152 % 10 = 2
So 1290604-86-2 is a valid CAS Registry Number.

1290604-86-2Downstream Products

1290604-86-2Relevant academic research and scientific papers

Synthesis and evaluation of new chalcones, derived pyrazoline and cyclohexenone derivatives as potent antimicrobial, antitubercular and antileishmanial agents

Monga, Vikramdeep,Goyal, Kamya,Steindel, Mario,Malhotra, Manav,Rajani, Dhanji P.,Rajani, Smita D.

, p. 2019 - 2032 (2014/05/06)

A series of chalcones (1-8) were prepared by Claisen-Schmidt condensation of 3-nitroacetophenone with various aldehydes. These chalcones on cyclization with hydrazine hydrate in the presence of glacial acetic acid, hydrazine hydrate in absolute ethanol an

Effect of ring A and ring B substitution on the cytotoxic potential of pyrazole tethered chalcones

Nepali, Kunal,Kadian, Kanika,Ojha, Ritu,Dhiman, Rajni,Garg, Atul,Singh, Gagandip,Buddhiraja, Abhishek,Bedi, Preet Mohinder Singh,Dhar, Kanaya Lal

, p. 2990 - 2997 (2012/10/29)

Chalcone is an aromatic ketone that forms the central core for a variety of important biological compounds, which are collectively known as chalcones. The cytotoxic potential of chalcones which consists of C6-C 3-C6 units gets enhanced by the incorporation of pyrazole ring as proved by our earlier studies. Thus in the present work, pyrazoles of chalcones with ring A substituted by furan, naphthalene and variety of substituted phenyl rings has been prepared and evaluated for in vitro cytotoxic activity against PC-3, OVCAR, IMR-32, HEP-2 human cancer cell lines. Springer Science+Business Media, LLC 2011.

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