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

60254-13-9

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60254-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60254-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,5 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60254-13:
(7*6)+(6*0)+(5*2)+(4*5)+(3*4)+(2*1)+(1*3)=89
89 % 10 = 9
So 60254-13-9 is a valid CAS Registry Number.

60254-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-hydroxyphenyl)methyl-diphenylphosphanium,iodide

1.2 Other means of identification

Product number -
Other names o-Hydroxyphenyl-diphenyl-methyl-phosphoniumiodid

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:60254-13-9 SDS

60254-13-9Downstream Products

60254-13-9Relevant academic research and scientific papers

Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts

Büttner, Hendrik,Steinbauer, Johannes,Werner, Thomas

, p. 2655 - 2669 (2015)

Numerous bifunctional organocatalysts were synthesized and tested for the atom-efficient addition of carbon dioxide and epoxides to produce cyclic carbonates. These catalysts are based on phosphonium salts containing an alcohol moiety in the side chain for substrate activation through hydrogen bonding. In the model reaction, converting 1,2-butylene oxide with CO2, 19 catalysts were tested to determine structure-activity relationships. In total, 28 epoxides were converted with CO2 to give the respective cyclic carbonates in yields of up to 99%. Even at 45C, the most active catalyst was able to produce cyclic carbonates selectively in high yields. The carbonates were generally obtained as analytically pure products after simple filtration over silica gel. This single-component catalyst system works under neat and mild reaction conditions and tolerates several useful moieties. Two heads are better than one! Bifunctional organocatalysts are synthesized and tested in the catalytic reaction of epoxides and carbon dioxide to give the respective cyclic carbonates. Product formation is significantly increased by hydrogen-bond donation from the bifunctional phosphonium catalyst.

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