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

89607-44-3

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89607-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89607-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,0 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89607-44:
(7*8)+(6*9)+(5*6)+(4*0)+(3*7)+(2*4)+(1*4)=173
173 % 10 = 3
So 89607-44-3 is a valid CAS Registry Number.

89607-44-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-4-(4-(dimethylamino)phenyl)-2,4-dihydro-3-methylpyrano[2,3-c]pyrazole-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-amino-3-methyl-4-(4-dimethylaminophenyl)-2,4 dihydropyrano[2,3-c]pyrazole-5-carbonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89607-44-3 SDS

89607-44-3Relevant academic research and scientific papers

Sugarcane Bagasse Ash-Based Silica-Supported Boric Acid (SBA-SiO2-H3BO3): A Versatile and Reusable Catalyst for the Synthesis of 1,4Dihydropyrano[2,3c]pyrazole Derivatives

Kumar, A.,Pandey, A. K.,Shrivastava, S. C.

, p. 653 - 660 (2021/06/02)

Abstract: A simple, green, and efficient protocol has been developed for the synthesis of biologically active 1,4dihydropyrano[2,3c]pyrazole derivatives via one-pot four-component reaction of various substituted benzaldehydes, hydrazine hydrate or phenylh

Synthesis and characterization of pine-cone derived carbon-based solid acid: A green and recoverable catalyst for the synthesis of pyra-no_pyrazole, amino-benzochromene, amidoalkyl naphthol and thiazoli-dinedione derivatives

Ghorbani, Fatemeh,Pourmousavi, Seied Ali,Kiyani, Hamzeh

, p. 66 - 81 (2021/03/19)

In this report, SO3H-functionalized Carbon nanoparticles (Pine-SO3H) with high acid density have been synthesized by the thermal treatment of sulfuric acid with Pine-Cone as carbon-based at 180oC in a sealed autoclave in a

Green synthesis of pyrazolopyranopyrimidinone and pyranopyrazole derivatives using porphyrin-initiated amine-functionalized PolyBCMO dendritic polymer as sonocatalyst

Avudaiappan, Govindan,Unnimaya T., Jayaprakash,Asha, Pallikkattil,Unnikrishnan, Vettukattil,Sreekumar, Krishnapillai

, p. 197 - 209 (2019/12/24)

A novel porphyrin-initiated amine-functionalized poly-3,3-bis(chloromethyl)oxetane (PBCMO-amine) dendritic polymer was effectively synthesized. Characterization using the UV-vis, IR, NMR, PXRD, TG, and FE-SEM spectroscopy and microscopy enabled one to ass

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 (2020/04/17)

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

Green synthesis of pyranopyrazoles via biocatalytic one-pot Knoevenagel condensation–Michael-type addition–heterocyclization cascade in non-aqueous media

Pandey, Rajat,Pratap, Umesh,Shrivas, Prabhakar,Wankhade, Atul,Zodape, Sangesh

, (2020/03/23)

Abstract: An efficient, green and facile route for the one-pot four-component synthesis of pyranopyrazole derivatives through the condensation of the aromatic aldehydes, ethyl acetoacetate, malononitrile and hydrazine hydrate using baker’s yeast as biocat

Design and development of a new functionalized cellulose-based magnetic nanocomposite: preparation, characterization, and catalytic application in the synthesis of diverse pyrano[2,3-c]pyrazole derivatives

Maleki, Ali,Eskandarpour, Vahid

, p. 1459 - 1472 (2019/06/10)

In this work, a facile protocol for the preparation of a new cellulose-based functionalized magnetic nanocomposite catalyst is described. The structure and morphology of the prepared nanomaterial was characterized by scanning electron microscopy, energy-d

A highly efficient and reusable catalyst for the synthesis of 4H-benzo[b]pyran derivatives

Redouane, Mohamed Abdenour,Khiri-Meribout, Naima,Benzerka, Saida,Debache, Abdelmadjid

, p. 167 - 179 (2020/02/27)

A series of substituted 4H-pyrans derivatives were synthesized by a one-pot, multi-component reaction of aromatic aldehydes, malononitrile, and pyrazolone derivatives or active methylene carbonyl compounds such as dimedone, in the presence of 1,3-dimethyl

Synthesis and antimicrobial study of 1,4-dihydropyrano[2,3-c]pyrazole derivatives in the presence of amino-functionalized silica-coated cobalt oxide nanostructures as catalyst

Shahbazi, Shakiba,Ghasemzadeh, Mohammad Ali,Shakib, Pegah,Zolfaghari, Mohammad Reza,Bahmani, Mahmoud

, p. 172 - 179 (2019/06/18)

In this research a series of pyranopyrazoles were efficiently synthesized via the one-pot four-component reactions of ethyl acetoacetate, hydrazinehydrate, aldehydes and malononitrile in the presence of Co3O4@SiO2-tNH

Sodium gluconate: An efficient organocatalyst for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives

Khandebharad, Amol,Sarda, Swapnil,Soni, Mahesh,Agrawal, Brijmohan

, p. 331 - 340 (2019/11/29)

Sodium gluconate presented as a category of biomolecule found to be a proficient and recyclable organocatalyst for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives via one-pot multicomponent reaction of aryl aldehyde, malononitrile, ethyl acetoac

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