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[1]Benzopyrano[4,3-c]pyrazol-4(1H)-one, 3-methyl-1-(3-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110570-19-9

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110570-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110570-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,7 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110570-19:
(8*1)+(7*1)+(6*0)+(5*5)+(4*7)+(3*0)+(2*1)+(1*9)=79
79 % 10 = 9
So 110570-19-9 is a valid CAS Registry Number.

110570-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-(3-methylphenyl)chromeno[4,3-c]pyrazol-4-one

1.2 Other means of identification

Product number -
Other names [1]Benzopyrano[4,3-c]pyrazol-4(1H)-one,3-methyl-1-(3-methylphenyl)

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:110570-19-9 SDS

110570-19-9Downstream Products

110570-19-9Relevant academic research and scientific papers

Copper-catalyzed cyclization of 3-acylcoumarin hydrazone using air as the oxidant: Efficient synthesis of pyrazole-fused coumarin derivatives

Wang, Hui-Yan,Liu, Xue-Cheng,Huang, Zhi-Bin,Shi, Da-Qing

, p. 380 - 385 (2015/03/30)

An efficient, convenient Cu-catalyzed formation of chromeno[4,3-c]pyrazol-4(1H)-ones is reported. In this atom economic process, readily available 3-acylcoumarin hydrazone is oxidative cyclized by direct C-N bond formation. Air has been successfully used

Synthesis, anticancer activity and photophysical properties of novel substituted 2-oxo-2H-chromenylpyrazolecarboxylates

Kumar, J. Ashok,Saidachary,Mallesham,Sridhar,Jain, Nishant,Kalivendi, Shashi Vardhan,Rao, V. Jayathirtha,Raju, B. China

supporting information, p. 389 - 402 (2013/10/01)

2-Oxo-2H-chromenylpyrazolecarboxylates (8a-h and 12a-zb) have been synthesized by [3 + 2] cycloaddition of 2H-chromenophenylhydrazones (7a-h and 11a-w) with diethyl/dimethylbut-2-ynedioates. Phenylchromeno[4,3-c]pyrazol-4(1H) -ones (13i-n) were prepared from corresponding phenylhydrazones (7a-h) with catalytic amount of piperidine in presence of pyridine as a solvent at 100°C. All the synthesized compounds (8a-h, 12a-zb and 13a-n) were screened for anticancer activity against three human cancer cell lines such as prostate (DU-145), lung adenocarcinoma (A549), and cervical (HeLa) by standard MTT assay method. Further, photophysical properties (UV and fluorescence) for these compounds were discussed.

THE CORRECT SYNTHESIS OF 2,3-DIHYDRO-2-ARYL-4-R-BENZOPYRANOPYRAZOLE-3-ONES.

Colotta, Vittoria,Cecchi, Lucia,Melani, Fabrizio,Palazzino, Giovanna,Filacchioni, Guido

, p. 5165 - 5168 (2007/10/02)

The correct synthesis of the title compounds 1a-b and 2a-b is described.The claimed synthesis of 2a from 2-methyl-3-chromonecarbonitrile is shown not to lead to 2a, as previously reported but to 1,4-dihydro-1-phenyl-3-methylbenzopyranopyrazole-4

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