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2067-93-8

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2067-93-8 Usage

Description

(1E)-2,3-diphenyl-1-(phenylmethylidene)-1H-indene, also known as diphenyldidecahydronaphthalene, is an organic compound with the molecular formula C28H20. It is a yellowish solid that is insoluble in water but soluble in most organic solvents. (1E)-2,3-diphenyl-1-(phenylmethylidene)-1H-indene is known for its potential applications in various fields due to its unique chemical structure and properties.

Uses

Used in Dye Production:
(1E)-2,3-diphenyl-1-(phenylmethylidene)-1H-indene is used as a key intermediate in the production of dyes. Its aromatic structure and solubility in organic solvents make it suitable for creating a wide range of colorful dyes for various applications.
Used in Perfume Formulation:
(1E)-2,3-diphenyl-1-(phenylmethylidene)-1H-indene is also utilized as a starting material in the creation of perfumes. Its aromatic properties contribute to the development of unique and long-lasting fragrances.
Used in Organic Synthesis:
(1E)-2,3-diphenyl-1-(phenylmethylidene)-1H-indene serves as a valuable building block in organic synthesis. Its reactivity and structural features allow for the synthesis of a variety of complex organic molecules.
Used in Pharmaceutical Research:
(1E)-2,3-diphenyl-1-(phenylmethylidene)-1H-indene has been studied for its potential biological activities, including anti-inflammatory and anticancer properties. This makes it a promising candidate for further research and development in the pharmaceutical industry.
Used in Synthesis of Derivatives with Pharmaceutical Applications:
As a starting material, (1E)-2,3-diphenyl-1-(phenylmethylidene)-1H-indene has been used to synthesize various derivatives with potential pharmaceutical applications. Its versatility in chemical reactions enables the development of new compounds with therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 2067-93-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2067-93:
(6*2)+(5*0)+(4*6)+(3*7)+(2*9)+(1*3)=78
78 % 10 = 8
So 2067-93-8 is a valid CAS Registry Number.

2067-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1E)-1-benzylidene-2,3-diphenylindene

1.2 Other means of identification

Product number -
Other names 1-Benzyliden-2,3-diphenyl-inden

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:2067-93-8 SDS

2067-93-8Relevant articles and documents

Catalytic Dimerization of Alkynes via C-H Bond Cleavage by a Platinum-Silylene Complex

Innocent, Jean,Kato, Tsuyoshi,Ohta, Masaya,Tobisu, Mamoru,Yoshida, Tomoki

supporting information, p. 1678 - 1682 (2020/06/08)

The cyclodimerization of diphenylacetylene derivatives catalyzed by a platinum-silylene complex is reported. The reaction proceeds via the cleavage of a carbon-hydrogen bond at the position ortho to an alkynyl group, and no additives are needed. Platinum complexes bearing other common ligands, such as phosphines and NHCs, failed to promote this reaction, highlighting the utility of the silylene ligand in this reaction.

Rhodium carbonyl catalyzed carbonylation of unsaturated compounds. IV. Carbonylation and oligomerization of diphenylacetylene catalyzed by Co4(CO)12, Rh4(CO)12, and Ir4(CO)12 under pressure of carbon monoxide

Hong,Mise,Yamazaki

, p. 247 - 248 (2007/10/02)

In the presence of Co4(CO)12, Rh4(CO)12, and Ir4(CO)12 catalysts the reaction of diphenylacetylene (1) in 2-propanol under pressure of carbon monoxide gave the hydrocarbonylation products 2 and/or 3 and the oligomers 4 and/or 5, in which the ratios depended on the catalyst employed.

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