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Phosphoric acid, diethyl (3-methoxyphenyl)methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49640-94-0

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49640-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49640-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,4 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49640-94:
(7*4)+(6*9)+(5*6)+(4*4)+(3*0)+(2*9)+(1*4)=150
150 % 10 = 0
So 49640-94-0 is a valid CAS Registry Number.

49640-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name m-methoxybenzyl diethyl 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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:49640-94-0 SDS

49640-94-0Relevant academic research and scientific papers

Palladium/Xiao-Phos-Catalyzed Kinetic Resolution of sec-Phosphine Oxides by P-Benzylation

Dai, Qiang,Liu, Lu,Zhang, Junliang

supporting information, p. 27247 - 27252 (2021/11/17)

P-stereogenic tert- and sec-phosphines have wide applications in asymmetric catalysis, materials, and pharmaceutical chemistry, however, their practical synthesis still constitutes a significant challenge. Herein, a successful kinetic resolution of rac-se

Photochemistry of phosphate esters: An efficient method for the generation of electrophiles

Givens, Richard S.,Matuszewski, Bogdan,Athey, Phillip S.,Robert Stoner

, p. 6016 - 6021 (2007/10/02)

The photochemical cleavage of benzyl diethyl phosphates, 1a-g, has been examined in tert-butyl alcohol, which produces the corresponding benzyl tert-butyl ether as the major solvolysis product upon direct irradiation. The multiplicity of the reactive excited state has been established as the singlet state. Evidence favoring an intermediate benzyl cation-phosphate ion pair formed from photofragmentation includes oxygen-18 scrambling, racemization of chiral benzyl phosphates, and substituent effects on the rate of reaction. The existence of an electrophilic intermediate is further supported by a linear free energy relationship for the rate of disappearance of 1, kdis, with Hammett σ, which gave a ρ value of -0.90 and for the rate of appearance of 2, kapp, a Hammett ρ value of -0.97. Possible mechanisms including an electron transfer either before or after homolysis or simple heterolysis of the ester bond are evaluated.

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