28447-26-9

Basic information

• Product Name: DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE
• Synonyms: DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE;Dimethyl(phthalimidomethyl)phosphonate, 98 %;(1,3-Dioxo-2,3-dihydro-1H-isoindole-2-ylmethyl)phosphonic acid dimethyl ester;[(1,3-Dihydro-1,3-dioxo-2H-isoindol)-2-yl]methylphosphonic acid dimethyl ester;Dimethyl ((1,3-dioxoisoindolin-2-yl);DIMETHYL (PHTHALIMIDOMETHYL)PHOSPHONATE(WXG00098)
• CAS NO: 28447-26-9
• Molecular Formula: C₁₁H₁₂NO₅P
• Molecular Weight: 269.19
• Mol File: 28447-26-9.mol
• Article Data: 7

Chemical Properties

• Melting Point: 115-116°C
• Boiling Point: 400.7 °C at 760 mmHg
• Flash Point: 196.1 °C
• Appearance: /
• Density: 1.39 g/cm³
• Vapor Pressure: 1.25E-06mmHg at 25°C
• Refractive Index: 1.553
• BRN: 1476370
• CAS DataBase Reference: DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE(28447-26-9)
• EPA Substance Registry System: DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE(28447-26-9)

Safety Data

• Safety Statements: 22-24/25
• Hazardous Substances Data: 28447-26-9(Hazardous Substances Data)

Usage

General Description

DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE is a synthetic chemical compound that is used as a flame retardant and in the production of polyurethane foam and other plastics. It is also known by the trade name "BEEP," and is used as an additive in a variety of industrial applications. DIMETHYL PHTHALIMIDOMETHYLPHOSPHONATE is known for its high thermal stability and excellent flame retardant properties, making it a valuable component in the manufacturing of fire-resistant materials. It is important to handle this chemical with care and follow proper safety precautions, as it can be harmful if ingested or inhaled, and can cause skin and eye irritation.

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

Upstream product

• 5332-26-3 N-(bromomethyl)phtalimide 
• 1914-20-1 N-methoxyphthalimide 
• 121-45-9 phosphorous acid trimethyl ester 

Downstream Products

• 1445-69-8 2,3-dihydrophthalazine-1,4-dione 
• 50918-71-3 dimethyl (aminomethyl)phosphonate 

Relevant articles and documents

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

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

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

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