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778-66-5

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778-66-5 Usage

Description

1-METHYL-2,2-DIPHENYLETHYLENE is a chemical compound with the molecular formula C18H16. It is characterized by a methyl group attached to a diphenylethene structure, which consists of two phenyl rings connected by an ethylene bridge. 1-METHYL-2,2-DIPHENYLETHYLENE is known for its unique structural features and potential applications in various fields.

Uses

Used in Coal Product Analysis:
1-METHYL-2,2-DIPHENYLETHYLENE is used as a detection agent for identifying structural features of products derived from coal. Its ability to interact with specific components in coal-derived products makes it a valuable tool in the analysis and characterization of these materials.

Synthesis Reference(s)

Tetrahedron Letters, 15, p. 1105, 1974 DOI: 10.1016/S0040-4039(01)82418-7

Check Digit Verification of cas no

The CAS Registry Mumber 778-66-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 778-66:
(5*7)+(4*7)+(3*8)+(2*6)+(1*6)=105
105 % 10 = 5
So 778-66-5 is a valid CAS Registry Number.

778-66-5SDS

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 1-phenylprop-1-enylbenzene

1.2 Other means of identification

Product number -
Other names 2-methyl-1,1-diphenylethylene

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:778-66-5 SDS

778-66-5Relevant articles and documents

An expedient route to tricyanovinylindoles and indolylmaleimides fromo-alkynylanilines utilising DMSO as a one-carbon synthon

Chakraborty, Nikita,Dahiya, Anjali,Modi, Anju,Patel, Bhisma K.,Rakshit, Amitava

supporting information, p. 6847 - 6857 (2021/08/20)

A Pd(ii)/Cu(ii) catalysed domino synthesis of tricyanovinylindoles has been achieved using DMSO as a one-carbon synthon. The reaction proceedsviathe construction of 2-aryl-3-formyl indole followed by sequential addition of malononitrile and a CN resulting

Photoredox-Catalyzed α-Aminomethyl Carboxylation of Styrenes with Sodium Glycinates: Synthesis of γ-Amino Acids and γ-Lactams

Zhou, Cong,Li, Miao,Sun, Jianwei,Cheng, Jiang,Sun, Song

supporting information, p. 2895 - 2899 (2021/05/05)

A visible-light photoredox-catalyzed reductive α-aminomethyl carboxylation of styrenes with sodium glycinates and CO2 has been developed to synthesize a series of α,α-disubstituted γ-amino acids and γ-lactams with high efficiency and regioselectivity. Notably, CO2 released from the decarboxylation step can be reused for the subsequent carboxylation. Distinct from the previous reactions with the same type of substrates leading to simple decarboxylation and olefin hydroalkylation, this process involves additional CO2 sequestration, thus leading to olefin α-aminomethyl carboxylation. These findings not only provide new access to α,α-disubstituted γ-amino acids and γ-lactams but also serve as a proof of concept for CO2 reutilization in decarboxylation reactions.

Visible-Light-Induced Meerwein Fluoroarylation of Styrenes

Tang, Hai-Jun,Zhang, Bin,Xue, Fei,Feng, Chao

supporting information, p. 4040 - 4044 (2021/05/26)

An unprecedented approach for assembling a broad range of 1,2-diarylethane derivatives with fluorine-containing fully substituted carbon centers was developed. The protocol features straightforward operation, proceeds under metal-free condition, and accommodates a large variety of synthetically useful functionalities. The critical aspect to the success of this novel transformation lies in using aryldiazonium salts as both aryl radical progenitor and also as single electron acceptor which elegantly enables a radical-polar crossover manifold.

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