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1H-Inden-1-one, 3-methoxy-2-phenyl- is an organic compound with the molecular formula C15H12O2. It is a derivative of inden-1-one, featuring a methoxy group at the 3-position and a phenyl group at the 2-position. 1H-Inden-1-one, 3-methoxy-2-phenyl- is characterized by its aromatic structure and is used in various chemical reactions and synthesis processes. It is an important intermediate in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is known for its unique properties, such as its reactivity and stability, which make it a valuable building block in organic synthesis.

2136-67-6

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2136-67-6 Usage

Classification

Aromatic ketone

Substituents

Methoxy group and phenyl group attached to the indenone ring

Usage

Organic synthesis, pharmaceutical research, and as a building block for the synthesis of other organic compounds

Biological activities

Antitumor, anti-inflammatory, and antimicrobial properties

Potential applications

Development of new drug molecules and as a research tool in medicinal chemistry

Value

Considered a valuable intermediate in the production of pharmaceuticals and fine chemicals

Check Digit Verification of cas no

The CAS Registry Mumber 2136-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2136-67:
(6*2)+(5*1)+(4*3)+(3*6)+(2*6)+(1*7)=66
66 % 10 = 6
So 2136-67-6 is a valid CAS Registry Number.

2136-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxy-2-phenyl-1H-inden-1-on

1.2 Other means of identification

Product number -
Other names 3-methoxy-2-phenyl-2-inden-1-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:2136-67-6 SDS

2136-67-6Relevant academic research and scientific papers

Ozonolysis of enol ethers. Part 10. Ozonization of enol ethers from 1,2- and 1,3-dicarbonyl compounds: Direct quantitative synthesis of phthalonic acid anhydride

Schank, Kurt,Beck, Horst,Pistorius, Susanne

, p. 2025 - 2049 (2007/10/03)

The results of ozonolyses of enol ethers from 1.2- and 1.3-dicarbonyl compounds presented here strongly indicate that these reactions do not proceed via the established Criegee ozonolysis mechanism for nucleophilic C=C bonds. The quantitative one-step synthesis of phthalonic acid anhydride via ozonolysis of 2-(methoxymethyliden)-1H-inden-1.3(2H)-dione (28a) is described. Furthermore, a revision of the theory of alkene ozonolysis in the presence of tetracyanoethylene (TCNE) is proposed on the basis of a single-electron-transfer (SET) chemistry.

On the synthesis of 2-substituted (η6-indan-1,3-dione)tricarbonylchromium complexes

Hrnciar, Peter,Hrnciar, Pavel,Gajda, Vladimir,Svanygova, Eva,Toma, Stefan

, p. 479 - 493 (2007/10/03)

Classical methods for the synthesis of indan-1,3-dione derivatives failed when applied to their tricarbonylchromium complexes. The desired 2-substituted (n6-indan- 1,3-dione)tricarbonylchromium complexes were prepared starting from protected in

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