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Phosphoric acid, diethyl 4-formyl-2-methoxyphenyl ester, also known as diethyl (4-formyl-2-methoxyphenyl) phosphate, is a complex organic compound with the chemical formula C11H15O6P. It is a derivative of phosphoric acid, featuring a 4-formyl-2-methoxyphenyl group esterified to the phosphoric acid backbone. This molecule is characterized by its ability to act as a phosphorylating agent, which can be used in the synthesis of various organic compounds, particularly in the preparation of pharmaceuticals and agrochemicals. The compound's structure includes a diethyl phosphate group connected to a substituted phenyl ring, which contributes to its reactivity and potential applications in chemical research and industry.

4799-60-4

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4799-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4799-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4799-60:
(6*4)+(5*7)+(4*9)+(3*9)+(2*6)+(1*0)=134
134 % 10 = 4
So 4799-60-4 is a valid CAS Registry Number.

4799-60-4SDS

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 diethyl (4-formyl-2-methoxyphenyl) phosphate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:4799-60-4 SDS

4799-60-4Relevant academic research and scientific papers

Microwave-assisted cleavage of phosphate, phosphonate and phosphoramide esters

Kishore Kumar,Saenz, David,Lokesh,Natarajan, Amarnath

, p. 6281 - 6284 (2007/10/03)

A mild and rapid protocol for cleavage of phosphate, phosphonate and phosphoramide esters. The scope and limitations of this microwave-assisted reaction is explored here.

Diethyl chlorophosphite: A versatile reagent

Jie, Zhou,Rammoorty, Vebumani,Fischer, Bilha

, p. 711 - 719 (2007/10/03)

Diethyl chlorophosphite (DECP) was previously described as a reducing agent for nitro compounds to the corresponding amines (Fischer, B.; Sheihet, L. J. Org. Chem. 1998, 63, 393). Here, the utility of this reagent was extended to chemical conversions of other oxygenated functional groups. In this paper we report on the scope of the reaction of DECP with N-oxides, epoxides, sulfones, sulfoxides, hydroxylamines, ketoximes, and aldoximes. The chemoselectivity of DECP is described, and conditions for a stepwise multiple conversion of functional groups on the same molecule with this reagent are provided.

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