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28447-26-9

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  • Phosphonic acid,P-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl]-, dimethyl ester

    Cas No: 28447-26-9

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28447-26-9 Usage

Description

DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE, also known as BEEP, is a synthetic chemical compound characterized by its high thermal stability and excellent flame retardant properties. It is a valuable component in the manufacturing of fire-resistant materials and is used as an additive in various industrial applications.

Uses

Used in Flame Retardant Industry:
DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE is used as a flame retardant for its ability to prevent or slow down the spread of fire in materials, enhancing their fire resistance.
Used in Plastics and Polyurethane Foam Production:
DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE is used as a key component in the production of polyurethane foam and other plastics, contributing to their flame retardant properties and improving their safety in various applications.
Used in Industrial Applications:
DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE is used as an additive in a variety of industrial applications, providing enhanced thermal stability and flame retardancy to the products.
It is important to handle DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE with care and follow proper safety precautions, as it can be harmful if ingested or inhaled, and can cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 28447-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,4 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28447-26:
(7*2)+(6*8)+(5*4)+(4*4)+(3*7)+(2*2)+(1*6)=129
129 % 10 = 9
So 28447-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H12NO5P/c1-16-18(15,17-2)7-12-10(13)8-5-3-4-6-9(8)11(12)14/h3-6H,7H2,1-2H3

28447-26-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L02840)  Dimethyl (phthalimidomethyl)phosphonate, 97%   

  • 28447-26-9

  • 2g

  • 448.0CNY

  • Detail
  • Alfa Aesar

  • (L02840)  Dimethyl (phthalimidomethyl)phosphonate, 97%   

  • 28447-26-9

  • 10g

  • 1484.0CNY

  • Detail
  • Alfa Aesar

  • (L02840)  Dimethyl (phthalimidomethyl)phosphonate, 97%   

  • 28447-26-9

  • 50g

  • 5708.0CNY

  • Detail

28447-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethoxyphosphorylmethyl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names dimethyl [(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl]phosphonate

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:28447-26-9 SDS

28447-26-9Relevant articles and documents

Michaelis-Arbuzov-type reaction of 1-imidoalkyltriarylphosphonium salts with selected phosphorus nucleophiles

Adamek, Jakub,egrzyk-Schlieter, Anna W.,Ste?, Klaudia,Walczak, Krzysztof,Erfurt, Karol

, (2019/09/30)

In this study, Michaelis-Arbuzov-type reaction of 1-imidoalkyltriarylphosphonium salts with phosphites, phosphonites, and phosphinites was used in the synthesis of a wide range of phosphorus analogs of α-amino acids such as 1-imidoalkylphosphonates, 1-imidoalkylphosphinates, and 1-imidoalkylphosphine oxides. Large differences were observed in the reactivity of substrates depending on their structure, especially on the type of phosphonium moiety and N-protecting group. The conditions under which the expected products can be obtained in good to excellent yields have been developed. Mechanistic aspects of the transformation have been provided.

Inhibitors of β-lactamase

-

, (2008/06/13)

The intention relates to bacterial antibiotic resistance and, in particular, to compositions and methods for overcoming bacterial antibiotic resistance. The invention provides novel β-lactamase inhibitors, which are structurally unrelated to the natural p

Novel Inhibitors of beta-lactamase

-

, (2008/06/13)

The invention relates to bacterial antibiotic resistance and, in particular, to compositions and methods for overcoming bacterial antibiotic resistance. The invention provides novel β-lactamase inhibitors, which are structurally unrelated to the natural p

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