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5-methyl-4-[(3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-yl)methyl]-2-phenyl-4H-pyrazol-3-one is a complex organic compound with a molecular formula of C22H18N4O2. It is a derivative of pyrazole, a heterocyclic compound with a five-membered ring containing three nitrogen atoms. This specific compound features a 5-methyl group, a 3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-ylmethyl group, and a 2-phenyl group attached to the pyrazole core. The compound is characterized by its unique structure and potential applications in various fields, such as pharmaceuticals and materials science. Its chemical properties and reactivity are influenced by the presence of the methyl and phenyl groups, as well as the oxo and pyrazole moieties.

7149-40-8

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7149-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7149-40-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7149-40:
(6*7)+(5*1)+(4*4)+(3*9)+(2*4)+(1*0)=98
98 % 10 = 8
So 7149-40-8 is a valid CAS Registry Number.

7149-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-Methylenbis(2-methyl-1-naphthol)

1.2 Other means of identification

Product number -
Other names 5,5'-dimethyl-2,2'-diphenyl-1,2,1',2'-tetrahydro-4,4'-methanediyl-bis-pyrazol-3-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

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

More Details:7149-40-8 SDS

7149-40-8Downstream Products

7149-40-8Relevant academic research and scientific papers

Extraction Ability of 5-Methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one and Bis(5-hydroxy-3-methyl-1-phenylpyrazol-4-yl)alkanes Derived from It

Degtev,Morozova,Smirnov

, p. 704 - 709 (2007/10/03)

Bis(5-hydroxy-3-methyl-1-phenylpyrazol-4-yl)alkanes were synthesized and shown to exist in polar solvents in the enol form, in contrast to the parent 5-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one. In order to determine centers of coordination in their re

STUDIES WITH POLYFUNCTIONALLY SUBSTITUTED HETEROCYCLES: SYNTHESIS OF NEW THIOPYRANS, PYRIDINES AND PYRANS AND THEIR FUSED DERIVATIVES WITH OTHER RINGS SYSTEMS

Elnagdi, Mohamed Hilmy,Ghozlan, Said Ahmed Soliman,Abdelrazek, Fathy Mohamed,Selim, Maghraby Ali

, p. 1021 - 1032 (2007/10/02)

The thiopyran derivative 3 was obtained from the reaction of cyanothioacetamide 2 with formaldehyde and malononitrile.Compound 3 is converted into the pyridinethione 5 on long reflux in ethanolic triethylamine solution.The pyridinethione 7 is produced from reaction of 2 with acetaldehyde and malononitrile.Compound 7 afforded 9 on reaction with 1a, R = Ph, and 11 on treatment with phenacyl bromide.The pyran derivative 13, formed in analogous manner from 12, afforded 19 on further reaction with formaldehyde and malononitrile, and 22 on reaction with acetic anhydride.Whereas the pyranopyrazole 27 is formed from 25a on reaction with formaldehyde and malononitrile in refluxing ethanol, 25b afforded only 28 an similar treatment.Similarly, thiazolopyridine derivative 30 and phthalazine 32 were formed from 29 and 31 respectively.

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