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2-[(4,4-dimethyl-2,6-dioxo-cyclohexyl)-(4-methoxyphenyl)methyl]-5,5-dimethyl-cyclohexane-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19419-24-0 Structure
  • Basic information

    1. Product Name: 2-[(4,4-dimethyl-2,6-dioxo-cyclohexyl)-(4-methoxyphenyl)methyl]-5,5-dimethyl-cyclohexane-1,3-dione
    2. Synonyms:
    3. CAS NO:19419-24-0
    4. Molecular Formula: C24H30O5
    5. Molecular Weight: 398.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19419-24-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 568°Cat760mmHg
    3. Flash Point: 245.1°C
    4. Appearance: N/A
    5. Density: 1.134g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(4,4-dimethyl-2,6-dioxo-cyclohexyl)-(4-methoxyphenyl)methyl]-5,5-dimethyl-cyclohexane-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(4,4-dimethyl-2,6-dioxo-cyclohexyl)-(4-methoxyphenyl)methyl]-5,5-dimethyl-cyclohexane-1,3-dione(19419-24-0)
    11. EPA Substance Registry System: 2-[(4,4-dimethyl-2,6-dioxo-cyclohexyl)-(4-methoxyphenyl)methyl]-5,5-dimethyl-cyclohexane-1,3-dione(19419-24-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 19419-24-0(Hazardous Substances Data)

19419-24-0 Usage

Cyclic molecule

Cyclohexane ring
The compound has a six-carbon ring structure in its core, known as a cyclohexane ring.

Functional groups

Methyl and methoxy groups
The compound contains methyl (CH3) and methoxy (OCH3) groups, which are responsible for its chemical reactivity and properties.
4. Complex organic compound
The compound has a complex structure with multiple functional groups and a cyclic core, making it a complex organic molecule.

Potential applications

Organic synthesis, pharmaceutical research, specialty chemicals
The compound may be used in various fields, such as creating new organic compounds, developing pharmaceuticals, or producing specialty chemicals.

Further research needed

Specific properties, uses, and potential risks
To fully understand the compound's behavior, applications, and safety, additional research and analysis are required.

Check Digit Verification of cas no

The CAS Registry Mumber 19419-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,1 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19419-24:
(7*1)+(6*9)+(5*4)+(4*1)+(3*9)+(2*2)+(1*4)=120
120 % 10 = 0
So 19419-24-0 is a valid CAS Registry Number.

19419-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4,4-dimethyl-2,6-dioxocyclohexyl)-(4-methoxyphenyl)methyl]-5,5-dimethylcyclohexane-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-(p-methoxyphenyl)methylenebis(5,5-dimethyl-1,3-cyclohexanedione)

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:19419-24-0 SDS

19419-24-0Relevant articles and documents

Application of SiO 2 nanoparticles as an efficient catalyst to develop syntheses of perimidines and tetraketones

Alinezhad, Heshmatollah,Ahmadi, Armin,Hajiabbasi, Parvin

, (2019/04/10)

Abstract: In this paper, we explore the catalytic activity of SiO 2 nanoparticles (NPs) as an eco-friendly, efficient and reusable catalyst in the synthesis of 2,3-dihydro-1H-perimidines as well as tetraketones. For tetraketones syntheses, a si

Merging supramolecular catalysis and aminocatalysis: Amino-appended β-cyclodextrins (ACDs) as efficient and recyclable supramolecular catalysts for the synthesis of tetraketones

Ren, Yufeng,Yang, Bo,Liao, Xiali

, p. 22034 - 22042 (2016/03/08)

Well-designed amino-appended β-cyclodextrins (ACDs) with an amino side chain of different lengths at the primary face of β-CD were synthesized and employed in the catalytic synthesis of a series of tetraketones as supramolecular catalysts in water for the first time. Yields of 58-97% were obtained with up to 30 examples of substrate. The catalyst could be recycled easily, while a 92% yield and 84% rate of catalyst recovery could be achieved after 8 cycles of catalyst recycling. Moreover, a catalytic mechanism merging supramolecular catalysis and aminocatalysis could be proposed through detailed 1D and 2D NMR, ESI-MS and Job plot analyses. This protocol retained the promising characteristics of ambient temperature, green medium, simple operation, broad substrate scope, excellent yields, superb catalyst recycling performance and unique catalytic mechanism.

A four-ketone derivative and its preparation method and application

-

Paragraph 0027; 0028; 0029, (2016/10/10)

The invention provides tetrone derivatives as well as a preparation method and application thereof. The derivatives have a general formula structure shown in the specification, wherein in the structure, R1 is any one of -H, 4-OCH3, 2-Cl, 3,4-(OCH3)2, 4-CH

L-Proline-catalysed the synthesis of aromatic aldehydes and ketones and their acridione derivatives at room temperature

Wang, Fang-Ming,Bao, Dan,Hu, Bing-Xiang,Zhou, Ze-Yu,Huang, Deng-Deng,Chen, Li-Zhuang,Liu, Yang-Mei

, p. 445 - 450 (2015/11/03)

A series of xanthene derivatives were prepared from cyclohexane-1,3-dione and aromatic aldehydes through Knoevenagel-Michael and cyclisation reactions in methanol:ethanol mixture (1:1), catalysed by a very small amount of l-proline at room temperature. Is

Aldonitrones as aldehyde equivalents: An efficient, green, and novel protocol for the synthesis of 1,8-dioxo-octahydroxanthenes

Kumar, Dhruva,Suresh,Sandhu, Jagir S.

, p. 2739 - 2747 (2013/08/23)

A novel, self-catalyzed, solvent-free, microwave-enhanced, green, and efficient protocol for the synthesis of 1,8-dioxo-octahydroxanthenes and bis-5,5-dimethyl-1,3-cyclohexanediones by condensing aldo-nitrones (imine oxide) and dimedone (5,5-dimethyl-1,3-

A green and highly efficient protocol for catalyst-free Knoevenagel condensation and Michael addition of aromatic aldehydes with 1,3-cyclic diketones in PEG-400

Firouzeh, Nemati,Hossein, Kiani

experimental part, p. 2407 - 2410 (2012/02/04)

A convenient, highly efficient and green approach for synthesis of tetraketones from aromatic aldehydes with dimedone and 1,3-indanedione at room temperature in PEG-400 is described. The use of PEG-400 as the reaction medium and avoiding the use of any ca

An efficient and simple synthesis of tetraketones catalyzed by Yb(OTf) 3-sio2 under solvent free conditions

Kameshwara Rao,Kumar, Muthyala Manoj,Kumar, Anil

experimental part, p. 1128 - 1135 (2011/10/04)

A novel and efficient three-component one-pot condensation method has been described for the synthesis of tetraketones or arylmethylene[bis(3-hydroxy-2- cyclohexene-1-ones)] using Yb(OTf)3-SiO2 and amine as catalytic system under sol

Fluorescence spectroscopic evidence for hydrogen bonding and deprotonation equilibrium between fluoride and a thiourea derivative

Ashokkumar, Pichandi,Ramakrishnan, Vayalakkavoor T.,Ramamurthy, Perumal

experimental part, p. 13271 - 13277 (2011/02/24)

Interaction of anions with thiourea-linked acridinedione fluorophore was studied by absorption, 1H NMR, steady-state and time-resolved fluorescence techniques. Addition of AcO- and H2PO 4- shows a gen

Synthesis and laser activity of halo-acridinedione derivatives

Kaya, Muharrem,Yildirir, Yilmaz,Tuerker, Lemi

experimental part, p. 294 - 297 (2009/07/19)

Synthesis of 10-(halophenyl)-9-(4-methoxyphenyl)-3, 4, 6, 7, 9, 10-hexahydroacridine-1, 8-(2H, 5H)-dione derivates have been prepared and their absorption, emission, and laser properties have been evaluated. The structures of all the synthesized compounds

Three component condensation of 6-quinolylamine with aromatic aldehydes and cyclohexyl 1,3-diketones

Kozlov,Gusak,Tkachev

, p. 740 - 747 (2008/03/11)

A three component condensation of 6-quinolylamine with 4-bromo-or 4-methoxybenzaldehyde, and 1,3-cyclohexanedione or dimedone gave 12-(4-bromophenyl)-and 12-(4-methoxyphenyl)-9,9-dimethyl-8,9,10,12-tetrahydro- 7H-benzo[b][4,7]phenanthrolin-11-ones. The re

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