5464-68-6

Basic information

• Product Name: Phosphonic acid, (carbamoylmethyl)-, diethyl ester
• Synonyms: Diethyl carbamoylmethylphosphonate;Phosphonic acid, (carbamoylmethyl)-, diethyl ester;Diethyl((2-amino-2-oxo)ethyl)phosphonate, 95 %;(2-Amino-2-oxoethyl)phosphonic acid diethyl ester;(Diethoxyphosphinyl)acetamide;2-diethoxyphosphorylacetamide;2-diethoxyphosphorylethanamide;Diethyl [(2-amino-2-oxo)ethyl]phosphonate
• CAS NO: 5464-68-6
• Molecular Formula: C₆H₁₄NO₄P
• Molecular Weight: 195.15300
• Mol File: 5464-68-6.mol

Chemical Properties

• Melting Point: 78-80 °C
• Boiling Point: 338.9ºC at 760 mmHg
• Flash Point: 158.8ºC
• Appearance: /
• Density: 1.18g/cm3
• Vapor Pressure: 9.52E-05mmHg at 25°C
• Refractive Index: 1.442
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 15.46±0.40(Predicted)
• BRN: 1777584
• CAS DataBase Reference: Phosphonic acid, (carbamoylmethyl)-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, (carbamoylmethyl)-, diethyl ester(5464-68-6)
• EPA Substance Registry System: Phosphonic acid, (carbamoylmethyl)-, diethyl ester(5464-68-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 5464-68-6(Hazardous Substances Data)

Usage

Uses

Used in Pesticide Applications:
Phosphonic acid, (carbamoylmethyl)-, diethyl ester is used as a pesticide for its ability to inhibit the growth of various types of microorganisms, which is crucial in protecting crops from diseases and pests, thereby ensuring a healthy and productive agricultural yield.
Used in Corrosion Inhibition:
In the industrial sector, Phosphonic acid, (carbamoylmethyl)-, diethyl ester is utilized as a corrosion inhibitor for metal surfaces. It functions by chelating metal ions, thereby preventing them from causing corrosion, which is essential for maintaining the integrity and longevity of metal structures and equipment.
Used in Agricultural Industry:
Phosphonic acid, (carbamoylmethyl)-, diethyl ester is used as a protective agent in the agricultural industry to safeguard crops from microbial infections, enhancing their resistance and overall health.
Used in Industrial Applications:
In industrial applications, it is used as a corrosion prevention agent to extend the lifespan of metal surfaces and structures by preventing the detrimental effects of corrosion.
The diethyl ester form of the compound facilitates its easy application and distribution in various formulations, making it a practical choice for a wide range of uses. However, it is imperative to handle and store this chemical compound with care to avoid potential health and environmental risks.

InChI:InChI=1/C6H14NO4P/c1-3-10-12(9,11-4-2)5-6(7)8/h3-5H2,1-2H3,(H2,7,8)

Upstream product

• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 79-07-2 Chloroacetamide 
• 122-52-1 triethyl phosphite 
• 683-57-8 bromo-acetic acid amide 

Downstream Products

• 934-86-1 C-Cyclohexyliden-acetamid 
• 37176-88-8 [(E)-1-Carbamoyl-2-(4-nitro-phenyl)-vinyl]-phosphonic acid diethyl ester 
• 820-99-5 Hex-2-ensaeure-amid 
• 829-97-0 5-phenyl-penta-2,4-dienoic acid amide 
• 4439-11-6 3,3-diphenylacrylamide 
• 41468-36-4 diethyl (2-aminoethyl)phosphonate 
• 76132-52-0 (Z)-3-Phenyl-3-(4-pyridyl)acrylamide 
• 76132-52-0 (E)-3-Phenyl-3-(4-pyridyl)acrylamide 
• 90921-37-2 3-Phenyl-buten-2-saeureamid 
• 92454-24-5 (E,E)-4-ethyl-2,4-hexadienamide 
• 22363-89-9 N-(Phosphonoacetyl)amine 
• 621-79-4 cinnamamide 
• 7386-65-4 (2E)-3-phenylbut-2-enamide 
• 7386-65-4 (Z)-3-phenylbut-2-enamide 

Relevant articles and documents

COMPOSITIONS FOR THE TREATMENT OF HYPERTENSION AND/OR FIBROSIS

The present invention relates to a novel terphenyl compound and its use in the prophylactic and/or therapeutic treatment of hypertension and/or fibrosis.

Development of an oxazole conjunctive reagent and application to the total synthesis of siphonazoles

(Chemical Equation Presented) The preparation of 4-carbethoxy-5-methyl-2- (phenylsulfonyl)methyloxazole and its use in the elaboration of more complex oxazoles are described. A total synthesis of the unique natural products siphonazoles A and B, illustrates an application of this building block. A discussion of the biological activity of the siphonazoles is also presented.

Microwave irradiation in organophosphorus chemistry 1: The Michaelis-Arbuzov reaction

A diverse series of phosphonate esters have been prepared using a domestic microwave oven. The microwave enhanced Michaelis-Arbuzov reaction shows remarkable rate acceleration under microwave irradiation and allows the facile synthesis, and in certain cases easy workup, of alkyl, α-substituted and aryl phosphonates.