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1H-Inden-1-one, 2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro- is a complex organic compound with the molecular formula C17H16O3. It is a derivative of inden-1-one, featuring a 3,4-dimethoxyphenyl group attached to the 2-position via a methylene bridge. This molecule is characterized by its tricyclic structure, with two benzene rings and one cyclopentane ring. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a precursor in the production of certain drugs. Its chemical properties and reactivity are influenced by the presence of the dimethoxyphenyl group, which can participate in various chemical reactions, such as oxidation and reduction, due to its electron-donating nature.

5706-15-0

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5706-15-0 Usage

Molecular Structure

A complex organic compound derived from 1H-inden-1-one with a dimethoxyphenylmethylene group attached at the 2-position of the inden ring.

Physical Form

A yellowish solid.

Potential Applications

May be used as an intermediate in the synthesis of organic compounds, or have pharmaceutical or biological properties.

Chemical Reactivity

The presence of the dimethoxyphenylmethylene group suggests significant chemical reactivity and potential for diverse applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5706-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5706-15:
(6*5)+(5*7)+(4*0)+(3*6)+(2*1)+(1*5)=90
90 % 10 = 0
So 5706-15-0 is a valid CAS Registry Number.

5706-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3′′,4′′-dimethoxybenzylidene)indan-1-one

1.2 Other means of identification

Product number -
Other names [(dimethoxy-3,4 phenyl) methylene]-2 indanone-1

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:5706-15-0 SDS

5706-15-0Relevant academic research and scientific papers

Continuous flow solvent free organic synthesis involving solids (reactants/products) using a screw reactor

Sharma, Brijesh M.,Atapalkar, Ranjit S.,Kulkarni, Amol A.

supporting information, p. 5639 - 5646 (2019/10/22)

Here we report for the first-time various organic transformations such as aldol condensation, oxidation, nucleophilic substitutions, protection, acylations and coupling reactions using a mechanochemical approach at a controlled temperature using a single synthesis platform. Almost minimal solvents or solvent-free conditions are used, making it a very efficient and clean synthesis of various products. A jacketed screw reactor when operated at different temperatures (0 °C to 160 °C) and over a range of rotation speeds for changing the residence time (15 s-300 s) helped to achieve maximum conversion. This approach is also extended to the synthesis using substrates having different substitutions, heterocycles and steric hindrance.

An efficient synthesis and antimicrobial screening of new hybrid molecules containing coumarin and indenopyridine moiety

Brahmbhatt, Dinkar I.,Patel, Chirag V.,Bhila, Varun G.,Patel, Niraj H.,Patel, Apoorva A.

, p. 1596 - 1606 (2015/04/21)

A novel series of hitherto unknown 3-(4-aryl-5H-indeno[1,2-b]pyridin-2-yl)coumarin derivatives 3a-r have been synthesized by the reaction of 3-coumarinyl methyl pyridinium salts 1a-c with appropriate 2-arylidene-1-indanones 2a-f under Krohnke's reaction c

Modified Pyridine-Substituted Coumarins: A New Class of Antimicrobial and Antitubercular Agents

Giri, Rakesh R.,Lad, Hemali B.,Bhila, Varun G.,Patel, Chirag V.,Brahmbhatt

, p. 363 - 375 (2015/10/29)

Some new biologically potent coumarin derivatives 7a-f, 8a-f, and 9a-f bearing modified pyridine moieties (indeno[1,2-b]pyridine, 4-azaphenanthrene and benzofuro [3,2-b]pyridine) at the sixth position were designed and synthesized. All the synthesized com

Evaluation of silica-H2SO4 as an efficient heterogeneous catalyst for the synthesis of chalcones

Sultan, Aeysha,Raza, Abdul Rauf,Abbas, Muhammad,Khan, Khalid Mohammed,Tahir, Muhammad Nawaz,Saari, Nazamid

, p. 10081 - 10094 (2013/09/23)

We report an efficient silica-H2SO4 mediated synthesis of a variety of chalcones that afforded the targeted compounds in very good yield compared to base catalyzed solvent free conditions as well as acid or base catalyzed refluxing conditions.

Synthesis of some imidazolyl-substituted 2-benzylidene indanone derivatives as potent aromatase inhibitors for breast cancer therapy

Bansal, Ranju,Narang, Gaurav,Zimmer, Christina,Hartmann, Rolf W.

experimental part, p. 661 - 669 (2012/05/20)

The synthesis and aromatase inhibitory activity of a new series of 2-benzylidene indanones is presented. The imidazolyl-substituted indanones displayed potent aromatase inhibitory activity. The vanilloid-based derivative 2-[4-(3-imidazol-1-ylpropoxy)-3-me

Understanding solid/solid organic reactions

Rothenberg,Downie,Raston,Scott

, p. 8701 - 8708 (2007/10/03)

The concept of an organic reaction between two macroscopic solid particles is investigated. Thus, we study several reactions that have been recently reported to proceed "in the solid phase" and clearly show that, in most cases, grinding the two solid reactants together results in the formation of a liquid phase. This is true both for catalytic transformations (e.g., aldol condensations and oligomerization of benzylic compounds) and for noncatalytic reactions (Baeyer - Villiger oxidations, oxidative coupling of naphthols using iron chloride, condensation of amines and aldehydes to form azomethines, homo-etherification of benzylic alcohols using p-toluenesulfonic acid, and nuclear aromatic bromination with NBS). This liquefaction implies the existence of a eutectic mixture with Tfusion below ambient temperature (although both reagents have higher than ambient melting points). In cases where heating is required, it is again clear that a phase change (from solid to liquid) occurs, explaining the observed reaction kinetics. On the basis of 19 experimental examples, we discuss the possibility of solid-phase organic reactions and the implications of these findings to the reaction between two solid reagents. A general description of such reactive systems is proposed, based on a consideration of the potential for eutectic (or peritectic) formation between the constituents of the liquid phases that arise during the process of mechanical mixing of the solid reagents and products.

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