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4-(4-CHLORO-PHENYL)-3-METHYL-1-PHENYL-1H-INDENO[1,2-B]PYRAZOLO[4,3-E]PYRIDIN-5-ONE is a complex organic compound with the molecular formula C27H19ClN2O. It features a unique structure that includes a phenyl ring, a pyrazolo[4,3-e]pyridine ring, and an indeno[1,2-b]pyrazole ring. The compound is characterized by the presence of a 4-chlorophenyl group, a methyl group, and a phenyl group attached to the central core. This chemical is likely to be found in specialized applications due to its intricate structure, potentially in the field of pharmaceuticals or as an intermediate in the synthesis of other complex molecules. Its specific properties, such as solubility, stability, and reactivity, would depend on the context of its use and the conditions under which it is being studied or applied.

1009630-24-3

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  • 4-(4-Chlorophenyl)-3-methyl-1-phenyl-1H-indeno[1,2-b]pyrazolo[4,3-e]pyridin-5-one

    Cas No: 1009630-24-3

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1009630-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1009630-24-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,6,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1009630-24:
(9*1)+(8*0)+(7*0)+(6*9)+(5*6)+(4*3)+(3*0)+(2*2)+(1*4)=113
113 % 10 = 3
So 1009630-24-3 is a valid CAS Registry Number.

1009630-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorophenyl)-3-methyl-1-phenylindeno[2,1-e]pyrazolo[3,4-b]pyridine-5(1H)-one

1.2 Other means of identification

Product number -
Other names 4-(4-chlorophenyl)-3-methyl-1-phenylindeno[1,2-b]pyrazolo[4,3-e]pyridin-5(1H)-one

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

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More Details:1009630-24-3 SDS

1009630-24-3Downstream Products

1009630-24-3Relevant articles and documents

Pyrazolo-fused 4-azafluorenones as key reagents for the synthesis of fluorescent dicyanovinylidene-substituted derivatives

Orrego-Hernández, Jessica,Lizarazo, Carolina,Cobo, Justo,Portilla, Jaime

, p. 27318 - 27323 (2019/09/12)

A green process to access pyrazolo-fused 4-azafluorenones (indeno[1,2-b]pyrazolo[4,3-e]pyridines, IPP) 4a-xvia the three-component reaction between indan-1,3-dione (1), benzaldehydes 2 and 5-amino-1-arylpyrazoles 3 is described. These compounds were successfully used as precursors of the novel dicyanovinylidene derivatives 7a-d containing different acceptor (A) or donor (D) aryl groups at position 4 of its fused system. The structures of products obtained (4a-x and 7a-d) were determined based on NMR experiments, HRMS analysis, and X-ray diffraction studies for 7b. The photophysical and computational studies of 7a-d showed that these products are modulable ICT fluorophores, even some preliminary tests revealed that these compounds could be used as fluorescent chemodosimeters for cyanide detection.

Aqua mediated indium(III) chloride catalyzed synthesis of fused pyrimidines and pyrazoles

Khurana, Jitender M.,Chaudhary, Ankita,Nand, Bhaskara,Lumb, Anshika

experimental part, p. 3018 - 3022 (2012/08/08)

The utilization of water as solvent and indium trichloride as promoter for the three-component combinatorial synthesis of a variety of bioactive pyrimidine and pyrazole derivatives (2-10) from aldehydes, 1,3-dicarbonyl compounds, and electron-rich amino h

Three-component one-pot synthesis of indeno[2',1':5,6]pyrido[2,3-d]pyrazole derivatives in aqueous media

Shi, Da-Qing,Shib, Jing-Wen,Yaob, Hao

experimental part, p. 504 - 509 (2010/06/11)

Aseries of indeno[2',1':5,6]pyrido[2,3-d]pyrazoles was synthesized by the three-component reaction of aldehyde, 5-amino-3-methyl-1-phenylpyrazole and 1,3-indenedione in the presence of SDS in aqueous media. The structures were characterized by IR, 1

A facile synthesis of furo[3,4-e]pyrazolo[3,4-b]pyridine-5(7H)-one derivatives via three-component reaction in ionic liquid without any catalyst

Shi, Da-Qing,Yang, Fang,Ni, Sai-Nan

experimental part, p. 469 - 476 (2009/08/17)

(Chemical Equation Presented) A series of furo[3,4-e]pyrazolo[3,4-b] pyridine-5(7H)-one and indeno[2,1-e]pyrazolo[3,4-b]pyridine-5(1H)-one derivatives were synthesized via the three-component reaction of an aldehyde, 5-aminopyrazole and either tetronic ac

A novel and efficient one-pot synthesis of furo[3′,4′:5,6]pyrido[2,3-c]pyrazole derivatives using organocatalysts

Shi, Chun-Ling,Shi, Da-Qing,Kim, Sung Hong,Huang, Zhi-Bin,Ji, Shun-Jun,Ji, Min

, p. 2425 - 2432 (2008/09/18)

A novel approach to one-pot synthesis of dihydrofuro[3′,4′:5,6]pyrido[2,3-c]pyrazole and indeno[2′,1′:5,6]pyrido[2,3-c]pyrazole derivatives have been investigated using organocatalysts that are recyclable. This new protocol has the advantages of environme

Regioselective three-component synthesis of novel indeno[1,2-b]-pyrazolo[4, 3-e]pyridines-fused derivatives of 4-azafluorenone alkaloid

Quiroga, Jairo,Cobo, Debora,Insuasty, Braulio,Abonia, Rodrigo,Cruz, Silvia,Nogueras, Manuel,Cobo, Justo

, p. 155 - 159 (2008/09/18)

(Chemical Equation Presented) New fused indeno[1,2-b]pyridine derivatives have been prepared in a multicomponent reaction from benzaldehydes, indanedione and the appropriate aminoheteroaryl compound. The simple methodology permitted the syntheses of a ser

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