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Phosphonium, (2-hydroxyphenyl)triphenyl-, iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21230-91-1

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21230-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21230-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,3 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21230-91:
(7*2)+(6*1)+(5*2)+(4*3)+(3*0)+(2*9)+(1*1)=61
61 % 10 = 1
So 21230-91-1 is a valid CAS Registry Number.

21230-91-1SDS

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 (2-hydroxyphenyl)-triphenylphosphanium,iodide

1.2 Other means of identification

Product number -
Other names 2-hydroxyphenyl triphenylphosphonium iodide

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:21230-91-1 SDS

21230-91-1Relevant academic research and scientific papers

Methoxy Groups Increase Reactivity of Bifunctional Tetraarylphosphonium Salt Catalysts for Carbon Dioxide Fixation: A Mechanistic Study

Toda, Yasunori,Komiyama, Yutaka,Esaki, Hiroyoshi,Fukushima, Kazuaki,Suga, Hiroyuki

, p. 15578 - 15589 (2019/11/21)

The development of carbon dioxide fixation under mild conditions is a central theme in organic synthesis. Despite the tremendous progress in the field of organocatalysis in the past two decades, the coupling reactions of epoxides with carbon dioxide that proceed at atmospheric pressure at temperatures of less than 100 °C have remained challenging. In our aspirational studies of tetraarylphosphonium salts (TAPS) catalysis, we report here the bifunctional TAPS-catalyzed synthesis of five-membered cyclic carbonates by chemical fixation using 1 atm of carbon dioxide at 60 °C. Intriguing substituent effects of TAPS were observed, in which electron-donating groups enhanced their reactivity. In addition, the mechanism was thoroughly investigated by undertaking both experimental and theoretical studies, suggesting that the electronic properties of TAPS affect carbon dioxide insertion into halohydrin intermediates. The results provided fruitful information to understand the origin of the TAPS behavior, which would contribute to the design of novel catalysts for carbon dioxide capture.

Curing accelerator, epoxy resin composition, and semiconductor device

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Page 16; 30, (2008/06/13)

A curing accelerator which is suitable for various curable resin compositions, an epoxy resin composition having excellent curability, storage stability and fluidity, and a semiconductor device having excellent solder cracking resistance and moisture resi

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