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1,2-dihydro-4-((4-hydroxy-2-oxo-2H-chromen-3-yl)-(3-nitrophenyl)methyl)-5-methyl-2-phenylpyrazol-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1403907-70-9

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1403907-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403907-70-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,9,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1403907-70:
(9*1)+(8*4)+(7*0)+(6*3)+(5*9)+(4*0)+(3*7)+(2*7)+(1*0)=139
139 % 10 = 9
So 1403907-70-9 is a valid CAS Registry Number.

1403907-70-9Downstream Products

1403907-70-9Relevant academic research and scientific papers

Ca(II)-catalyzed, one-pot four component synthesis of functionally embellished benzylpyrazolyl coumarins in water

Yaragorla, Srinivasarao,Pareek, Abhishek,Dada, Ravikrishna

, p. 4770 - 4774 (2015)

A facile one-pot, four-component synthesis of biologically important benzylpyrazolyl coumarins in water has been demonstrated using environmentally benign Ca(II) as the catalyst. Participation of aliphatic aldehydes has been described for the first time. Short reaction times, high yields and chromatography free isolation of the products, usage of eco-friendly catalyst and solvent are the key features of this method.

A facile solvent-free route for one-pot multicomponent synthesis of benzylpyrazolyl coumarins derivatives in presence of effective synergetic catalytic system

Kamble, Narendra R.,Kamble, Vinod T.

, p. 1357 - 1361 (2019/06/10)

A combinatorial library of benzylpyrazolyl coumarin derivatives have been synthesized by a green one-pot four-component reaction between aryl hydrazine/hydrazine hydrate (1), ethyl acetoacetate (2), aromatic aldehydes (3) and 4-hydroxycoumarin (4) catalyz

Metal-free heterogeneous and mesoporous biogenic graphene-oxide nanoparticle-catalyzed synthesis of bioactive benzylpyrazolyl coumarin derivatives

Siddiqui,Ghule, Balaji G.,Shaikh, Shoyebmohamad,Shinde, Pritamkumar V.,Gunturu, Krishna Chaitanya,Zubaidha,Yun, Je Moon,O'Dwyer, Colm,Mane, Rajaram S.,Kim, Kwang Ho

, p. 17373 - 17379 (2018/05/29)

We report the preparation of graphene oxide nanoparticles (GONPs), a metal-free, heterogeneous, non-toxic, reusable and mesoporous green-(acid)-catalyst obtained by sugar carbonization through a micro-wave chemical synthesis method for the synthesis of bi

Design and synthesis of benzylpyrazolyl coumarin derivatives via a four-component reaction in water: Investigation of the weak interactions accumulating in the crystal structure of a signified compound

Ghosh, Partha Pratim,Pal, Gargi,Paul, Sanjay,Das, Asish R.

supporting information, p. 2691 - 2698 (2012/11/06)

A combinatorial library of benzylpyrazolyl coumarin derivatives have been synthesized by a green one-pot four-component reaction between aryl hydrazine/hydrazine hydrate (1), ethyl acetoacetate (2), aromatic aldehydes (3) and 4-hydroxycoumarin (4). Molecular scaffolds which assimilate bio-active 3-benzylsubstituted 4-hydroxycoumarins as well as a pyrazolone ring in a single nucleus may be worthwhile molecules from a biological point of view. The reactions were performed in water and employed glacial acetic acid as the right choice of catalyst, and was demonstrated to be the key for rendering the reaction possible and obtained good to excellent yields under reflux conditions within a short period of time. The crystal structures of (R/S)-benzylpyrazolyl coumarin, easily produced by a chromatography-free highly product-selective reaction, were explored by means of single crystal X-ray diffraction analysis and the main intra- and intermolecular interactions perceivable through crystal structure analysis. The presence of a strong intramolecular hydrogen bond was confirmed. In addition, the whole crystal structure consists of other intermolecular hydrogen bonds, such as CH...O and aromatic CH...π interactions between R- and S-molecules and CH...O, NH...O and aromatic CH...π interactions among only R-molecules and S-molecules in the asymmetric unit.

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