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10-Decyloxy-9,10-dihydro-9-oxa-10-phosphaphenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52458-38-5

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52458-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52458-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,5 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52458-38:
(7*5)+(6*2)+(5*4)+(4*5)+(3*8)+(2*3)+(1*8)=125
125 % 10 = 5
So 52458-38-5 is a valid CAS Registry Number.

52458-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-decoxybenzo[c][2,1]benzoxaphosphinine

1.2 Other means of identification

Product number -
Other names 10-Decyloxy-9,10-dihydro-9-oxa-10-phosphaphenanthrene

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:52458-38-5 SDS

52458-38-5Downstream Products

52458-38-5Relevant academic research and scientific papers

A novel and effective synthetic approach to 9,10-dihydro-9-oxa-10- phosphaphenanthrene-10-oxide (DOPO) derivatives

Artner, Johannes,Ciesielski, Michael,Ahlmann, Martin,Walter, Olaf,Doering, Manfred,Perez, Raul M.,Altstaedt, Volker,Sandler, Jan K. W.,Schartel, Bernhard

, p. 2131 - 2148 (2007)

DOPO and its derivatives generally exhibit an outstanding performance as flame retardants in various polymers. Starting from trivalent 10-alkoxy-10H-9-oxa-10-phosphaphenanthrenes, a broad range of DOPO derivatives was synthesized via transesterification with aliphatic alcohols and subsequent Michaelis-Arbuzov rearrangement using catalytic amounts of p-toluenesulfonic acid methylester. Due to the considerable differences in the nature of the alcohols employed, several procedures for processing them are presented.

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