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Phosphonium, [1-(ethoxycarbonyl)-3-butenyl]triphenyl-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110189-66-7

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110189-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110189-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110189-66:
(8*1)+(7*1)+(6*0)+(5*1)+(4*8)+(3*9)+(2*6)+(1*6)=97
97 % 10 = 7
So 110189-66-7 is a valid CAS Registry Number.

110189-66-7SDS

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 (1-ethoxy-1-oxopent-4-en-2-yl)-triphenylphosphanium,bromide

1.2 Other means of identification

Product number -
Other names Phosphonium,[1-(ethoxycarbonyl)-3-butenyl]triphenyl-,bromide

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:110189-66-7 SDS

110189-66-7Relevant academic research and scientific papers

Unique Reactivity of α-Substituted Electron-Deficient Allenes using Sulfinate Salts as Lewis Base Organocatalysts

Martzel, Thomas,Lohier, Jean-Fran?ois,Gaumont, Annie-Claude,Brière, Jean-Fran?ois,Perrio, Stéphane

, p. 96 - 106 (2017)

The efficient sulfinate-catalyzed intermolecular addition reaction of α-substituted allenyl sulfones and allenoates with Michael acceptors is highlighted. The sequence proceeds under mild conditions to provide a scalable and efficient access to versatile

Phosphine-catalyzed annulations of azomethine imines: Allene-dependent [3 + 2], [3 + 3], [4 + 3], and [3 + 2 + 3] pathways

Na, Risong,Jing, Chengfeng,Xu, Qihai,Jiang, Hui,Wu, Xi,Shi, Jiayan,Zhong, Jiangchun,Wang, Min,Benitez, Diego,Tkatchouk, Ekaterina,Goddard, William A.,Guo, Hongchao,Kwon, Ohyun

supporting information; experimental part, p. 13337 - 13348 (2011/10/09)

In this paper we describe the phosphine-catalyzed [3 + 2], [3 + 3], [4 + 3], and [3 + 2 + 3] annulations of azomethine imines and allenoates. These processes mark the first use of azomethine imines in nucleophilic phosphine catalysis, producing dinitrogen

A CONVENIENT TWO-STEP SYNTHESIS OF 3-ALLYLCOUMARINS AND THEIR BENZODERIVATIVES

Mali, Raghao S.,Tilve, Santosh G.,Yeola, Suresh N.,Manekar, Anita R.

, p. 121 - 127 (2007/10/02)

A convenient, high yield, two step synthesis of 3-allylcoumarins and their benzo derivatives is described from 2-hydroxybenzaldehydes.The benzaldehydes (2a-j) on reaction with phosphorane 3 provide E-ethyl-α-allylcinnamates (4a-j) in high yields.These est

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