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1,3,2-Diazaphosphorinane, 2-oxide, 2-phenoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16456-52-3

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16456-52-3 Usage

Type of compound

Heterocyclic compound

Key elements

Phosphorus and nitrogen atoms

Ring structure

Six-membered ring

Functional group

Phenoxy group (benzene ring with an attached oxygen atom)

Application

Organic synthesis

Use as a building block

Preparation of various organic compounds

Potential applications

Pharmaceuticals and agrochemicals

Research areas

Medicinal chemistry and materials science

Check Digit Verification of cas no

The CAS Registry Mumber 16456-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,5 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16456-52:
(7*1)+(6*6)+(5*4)+(4*5)+(3*6)+(2*5)+(1*2)=113
113 % 10 = 3
So 16456-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N2O2P/c12-14(10-7-4-8-11-14)13-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2,(H2,10,11,12)

16456-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenoxy-1,3,2λ<sup>5</sup>-diazaphosphinane 2-oxide

1.2 Other means of identification

Product number -
Other names 2-phenoxy-[1,3,2]diazaphosphinane 2-oxide

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:16456-52-3 SDS

16456-52-3Downstream Products

16456-52-3Relevant academic research and scientific papers

Characterizing the thermal degradation mechanism of two bisphosphoramidates by TGA, DSC, mass spectrometry and first-principle theoretical protocols

Castrejón-Flores, José Luis,Flores-Martinez, Yazmin M.,Franco-Pérez, Marco,García-Ventura, María Isabel,Reyna-Luna, Julieta,Zamudio-Medina, Angel

, (2020/07/16)

The present investigation describes a combined experimental-theoretical strategy to assess the thermal resistance features of two symmetric bisphosphoramidates, tetraphenyl ethane-1,2-diylbis (phosphoramidate) 1 and tetraphenyl propane-1,3-diylbis (phosphoramidate) 5. Therefore, their structural reluctance to thermal decomposition through differential scan calorimetric (DSC) and thermogravimetric (TGA) experiments was evaluated. Then, their molecular degradation path was followed by analysing recorded data from mass spectrometry measurements performed at different temperature conditions. Their corresponding thermal degradation mechanism was then established by searching plausible transition states interconnecting the intermediaries found in our mass spectrometry records using a quantum theoretical protocol based on Coupled-Cluster calculations. Through this strategy, key intermediaries of the two bisphosphoramidates studied during their molecular degradation mechanism were identified, although compound 5 displayed the highest resistance to heat decomposition.

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