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124009-63-8

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124009-63-8 Usage

Description

3H-Pyrazol-3-one, 2,4-dihydro-4,4-bis(5-hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)-5-methyl-2-phenylis a complex organic compound with a unique structure that features a pyrazolone core and two pyrazolyl substituents. 3H-Pyrazol-3-one, 2,4-dihydro-4,4-bis(5-hydroxy-3-Methyl1-phenyl-1H-pyrazol-4-yl)-5-Methyl-2-phenylhas been synthesized through novel reactions and can be further studied for its potential applications in various fields.

Uses

Used in Chemical Synthesis:
3H-Pyrazol-3-one, 2,4-dihydro-4,4-bis(5-hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)-5-methyl-2-phenylis used as a key intermediate in the synthesis of various organic compounds, including 4-arylidene-3-methyl-1-phenyl-2-pyrazolin-5-one derivatives. Its unique structure and reactivity make it a valuable building block for the development of new molecules with potential applications in pharmaceuticals, materials science, and other industries.
Used in Pharmaceutical Research:
3H-Pyrazol-3-one, 2,4-dihydro-4,4-bis(5-hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)-5-methyl-2-phenylcan be studied for its potential pharmaceutical applications, given its complex structure and the presence of functional groups that may exhibit biological activity. Further research is needed to explore its potential as a therapeutic agent or as a lead compound for the development of new drugs.
Used in Materials Science:
The unique structure of 3H-Pyrazol-3-one, 2,4-dihydro-4,4-bis(5-hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)-5-methyl-2-phenylmay also find applications in materials science, where its properties can be harnessed to create new materials with specific characteristics. For example, it could be used in the development of advanced polymers, coatings, or other materials with tailored properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 124009-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,0 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124009-63:
(8*1)+(7*2)+(6*4)+(5*0)+(4*0)+(3*9)+(2*6)+(1*3)=88
88 % 10 = 8
So 124009-63-8 is a valid CAS Registry Number.

124009-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3',3''-Trimethyl-1,1',1''-triphenyl-4,4',4''-tris-(2-pyrazolin-5-on)

1.2 Other means of identification

Product number -
Other names 3H-Pyrazol-3-one, 2,4-dihydro-4,4-bis(5-hydroxy-3-Methyl- 1-phenyl-1H-pyrazol-4-yl)-5-Methyl-2-phenyl-

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:124009-63-8 SDS

124009-63-8Downstream Products

124009-63-8Relevant articles and documents

Electrochemical-Induced C(sp3)?H Dehydrogenative Trimerization of Pyrazolones to Tripyrazolones

Ma, Jing,Sun, Xue,Tian, Laijin,Wei, Wei,Wen, Jiangwei,Yan, Kelu,Yang, Jianjing

supporting information, p. 5491 - 5496 (2021/11/01)

The electrochemical-induced three-component C(sp3)?H dehydrogenative trimerization of pyrazolones to tripyrazolones with hydrogen evolution has been accomplished under the metal- and external-oxidant-free conditions. This protocol provides an efficient and eco-friendly method for the synthesis of tripyrazolones, which avoids the use of metals and stoichiometric chemical oxidants. A wide range of functional groups was tolerated to give selectively the desired products in high yields. Importantly, such an electrochemical-oxidation-induced dehydrogenative trimerization reaction could be easily scaled up with excellent efficiency.

"Furlongelb" - ein 1,3-Dioxepin-Derivat

Hennig, Lothar,Mann, Gerhard,Rissanen, Kari

, p. 59 (2007/10/02)

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