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2,4,6-Triphenyl-1,3,5,2,4,6-trioxatriphosphorinane 2,4,6-trioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57156-84-0

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57156-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57156-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,5 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57156-84:
(7*5)+(6*7)+(5*1)+(4*5)+(3*6)+(2*8)+(1*4)=140
140 % 10 = 0
So 57156-84-0 is a valid CAS Registry Number.

57156-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-triphenyl-1,3,5,2λ<sup>5</sup>,4λ<sup>5</sup>,6λ<sup>5</sup>-trioxatriphosphinane 2,4,6-trioxide

1.2 Other means of identification

Product number -
Other names 1,3,5,2,4,6-Trioxatriphosphorinane,2,4,6-triphenyl-,2,4,6-trioxide

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:57156-84-0 SDS

57156-84-0Downstream Products

57156-84-0Relevant academic research and scientific papers

Ring-Opening Polymerization of Cyclic Phosphonates: Access to Inorganic Polymers with a PV-O Main Chain

Arz, Marius I.,Annibale, Vincent T.,Kelly, Nicole L.,Hanna, John V.,Manners, Ian

supporting information, p. 2894 - 2899 (2019/03/05)

We describe a new class of inorganic polymeric materials featuring a main chain consisting of PV-O bonds and aryl side groups, which was obtained with >70 repeat units by ring-opening polymerization of cyclic phosphonates. This monomer-polymer system was found to be dynamic in solution enabling selective depolymerization under dilute conditions, which can be tuned by varying the substituents. The polymers show high thermal stability to weight loss and can be easily fabricated into self-standing thin films. Structural characterizations of the cyclic 6-and 12-membered ring precursors are also described.

New reactions of selenocarboxylates

Knapp, Spencer,Darout, Etzer

, p. 203 - 206 (2007/10/03)

(Chemical Equation Presented) By treatment with Woollins' reagent in toluene solution, carboxylic acids are converted to selenocarboxylic acids. The latter react in situ to provide new products of acid- or base-promoted substitution, addition, and amidation.

REACTIONS OF DICYANOPHOSPHINES WITH CARBOXYLIC ACIDS

Pudovik, A. N.,Nazmutdinova, V. N.,Chirkova, L. P.,Musin, R. Z.

, p. 221 - 224 (2007/10/02)

Acidolysis reactions of alkyl- and aryl-dicyanophosphines lead mainly to the formation of compounds with a P-P bond.A reaction scheme is proposed.

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