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"Benzene, 1,1',1''-(1-chloro-1,2-propadien-1-yl-3-ylidene)tris-" is a complex organic compound with the chemical formula C15H12Cl3. It is a derivative of benzene, where three 1-chloro-1,2-propadien-1-yl-3-ylidene groups are attached to the benzene ring. Benzene, 1,1',1''-(1-chloro-1,2-propadien-1-yl-3-ylidene)tris- is characterized by its unique structure, which features a chlorine atom and a conjugated diene system in each of the three substituents. It is an example of a polyhalogenated aromatic compound, which can have various applications in chemical synthesis and as intermediates in the production of other chemicals. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest in organic chemistry research.

2115-13-1

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2115-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2115-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2115-13:
(6*2)+(5*1)+(4*1)+(3*5)+(2*1)+(1*3)=41
41 % 10 = 1
So 2115-13-1 is a valid CAS Registry Number.

2115-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-1,3,3-triphenylallene

1.2 Other means of identification

Product number -
Other names 1-Chlor-1,3,3-triphenylallen

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:2115-13-1 SDS

2115-13-1Relevant academic research and scientific papers

The rubrenic synthesis: The delicate equilibrium between tetracene and cyclobutene

Braga, Daniele,Jaafari, Abdelhafid,Miozzo, Luciano,Moret, Massimo,Rizzato, Silvia,Papagni, Antonio,Yassar, Abderrahim

, p. 4160 - 4169 (2011/10/01)

Herein we describe the synthesis of new substituted tetraaryltetracenes, obtained by the dimerization of triarylchloroallenes, prepared from propargyl alcohols. The propargyl alcohols were prepared by two different synthetic strategies and then the alcohols were treated to obtain the corresponding acenes. In addition to the expected tetracene derivatives, we observed the formation of bis(alkylidene)cyclobutenes. When strong electron-donating substituents were present, the main product was the cyclobutene. We discuss a reaction mechanism that accounts for the formation of the cyclobutenes.

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