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6-amino-1,4-dihydro-3-methyl-4-(2-hydroxyphenyl)pyrano[2,3-c]pyrazole-5-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1189358-66-4

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1189358-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1189358-66-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,9,3,5 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1189358-66:
(9*1)+(8*1)+(7*8)+(6*9)+(5*3)+(4*5)+(3*8)+(2*6)+(1*6)=204
204 % 10 = 4
So 1189358-66-4 is a valid CAS Registry Number.

1189358-66-4Downstream Products

1189358-66-4Relevant academic research and scientific papers

Catalyst-free green synthesis of dihydropyrano[2,3-c]pyrazole scaffolds assisted by ethylene glycol (E-G) as a reusable and biodegradable solvent medium

Mohamadpour, Farzaneh

, (2020)

Abstract: We revealed a catalyst-free, green and rapid one-pot four-component tandem strategy for the preparation of dihydropyrano[2,3-c]pyrazoles – a biologically significant scaffold – via Knoevenagel-Michael cyclocondensation based on green chemistry p

An efficient catalyst- and solvent-free method for the synthesis of medicinally important dihydropyrano[2,3-c]pyrazole derivatives using ball milling technique

Dekamin, Mohammad G.,Alikhani, Mohammad,Emami, Atefeh,Ghafuri, Hossein,Javanshir, Shahrzad

, p. 591 - 596 (2016)

Dihydropyrano[2,3-c]pyrazole annulated heterocyclic compounds with diverse substituents on the 4H-pyran ring were efficiently prepared via a one-pot and four-component reaction of ethyl acetoacetate, hydrazine hydrate, aromatic aldehyde, and malononitrile

Morpholine triflate promoted one-pot, four-component synthesis of dihydropyrano[2,3-c]pyrazoles

Zhou, Chen-Feng,Li, Jian-Jun,Su, Wei-Ke

, p. 1686 - 1690 (2016)

A one-pot, four-component reaction of ethyl acetoacetate, hydrazine hydrate, aldehydes, and malononitrile was discussed using Lewis acid catalyst morpholine triflate (MorT) to afford a series of dihydropyrano[2,3-c]pyrazoles, which were generally catalyze

A four-component synthesis of dihydropyrano[2,3-c]pyrazoles in a new water-based worm-like micellar medium

Tamaddon, Fatemeh,Alizadeh, Masoomeh

, p. 3588 - 3591 (2014)

Cocamidopropyl betaine (CAPB) as a biodegradable surfactant produces a new worm-like micellar medium for rapid synthesis of dihydropyrano[2,3-c]pyrazoles via a four-component reaction of aldehydes, ethyl acetoacetate, malononitrile, and hydrazine hydrate

A green and one-pot synthesis of a library of 1,4-dihydropyrano[2,3-c]-pyrazole-5-carbonitrile derivatives using thiourea dioxide (TUD) as an efficient and reusable organocatalyst

Vekariya, Rajesh H.,Patel, Kinjal D.,Patel, Hitesh D.

, p. 4683 - 4696 (2016)

Abstract: The efficacy of thiourea dioxide (TUD) as an efficient, inexpensive, and readily accessible organocatalyst for the synthesis of 1,4-dihydropyrano[2,3-c]-pyrazole-5-carbonitrile derivatives via a four-component reaction of ethyl acetoacetate, hyd

Nano silica extracted from horsetail plant as a natural silica support for the synthesis of H3PW12O40 immobilized on aminated magnetic nanoparticles (Fe3O4@SiO2-EP-NH-HPA): a novel and effi

Hosseini Mohtasham, Nina,Gholizadeh, Mostafa

, p. 3037 - 3066 (2020)

Abstract: In this work, nanomesoporous silica has been prepared from horsetail (Equisetum arvense), which is a medicinal plant, with high surface area. This natural silica has been applied as a support to prepare H3PW12O40

An approach to the synthesis and characterization of HMS/Pr-Rh-Zr as efficient catalyst for synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives

Abdolahi, Sahar,Hajjami, Maryam,Gholamian, Fatemeh

, p. 1883 - 1904 (2021)

The aim of present investigation is the synthesis of mesoporous catalyst based on hexagonal mesoporous silica. HMS support has exceptional properties such as easy synthesis, high surface area, large pore volume and wormhole pores. These distinctive charac

Synthesis of pyrano[2,3-c]pyrazole derivatives using Fe3O4@SiO2@piperidinium benzene-1,3-disulfonate (Fe3O4@SiO2 nanoparticle-supported IL) as a novel, green and heterogeneous catalyst

Ghorbani-Vaghei, Ramin,Mahmoodi, Jafar,Shahriari, Azadeh,Maghbooli, Yaser

, (2017)

A simple, green and efficient protocol for the one-pot four-component synthesis of pyrano[2,3-c]pyrazole derivatives produced from reaction between aryl aldehydes, ethyl acetoacetate, malononitrile and hydrazine hydrate in the presence of nano magnetic piperidinium benzene-1,3-disulfonate was synthesized in water at 60 °C. The Fe3O4@SiO2 nanoparticle-supported IL was designed and synthesized. The present process offers advantages such as clean reaction, short reaction time, good to excellent yield, easy purification and easy recoverable catalyst.

DABA MNPs: A new and efficient magnetic bifunctional nanocatalyst for the green synthesis of biologically active pyrano[2,3-: C] pyrazole and benzylpyrazolyl coumarin derivatives

Karami, Shahriar,Dekamin, Mohammad G.,Valiey, Ehsan,Shakib, Peyman

, p. 13952 - 13961 (2020)

In this work, a new core-shell magnetic silica nanocatalyst functionalized with 3,4-diaminobenzoic acid (Fe3O4@SiO2@PTS-DABA) was successfully prepared and characterized using different spectroscopic methods or techniques including FT-IR, FE-SEM, VSM, XRD

Concentrated solar radiation-assisted one-pot/multicomponent synthesis of pyranopyrazole derivatives under neat condition

Gadkari, Yatin U.,Hatvate, Navnath T.,Telvekar, Vikas N.

, p. 4245 - 4255 (2021/07/17)

Concentrated solar radiation (CSR)-assisted synthesis of pyranopyrazole derivatives under solvent and catalyst-free condition has been reported in the present protocol. One-pot multicomponent synthesis from aromatic/heteroaldehyde, ethyl acetoacetate, malononitrile, and hydrazine hydrate leads to the final desired compounds in a good yield. This operationally simple methodology has several advantages such as green and clean reaction profile, simple workup and purification procedures, extremely short reaction time, atom efficiency, and being economical. The current energy-efficient method saves almost 98% of energy as compared to the conventional method. Graphical abstract: [Figure not available: see fulltext.]

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