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

59463-48-8

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59463-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59463-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,6 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59463-48:
(7*5)+(6*9)+(5*4)+(4*6)+(3*3)+(2*4)+(1*8)=158
158 % 10 = 8
So 59463-48-8 is a valid CAS Registry Number.

59463-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethoxyphosphorylmethoxy)acetonitrile

1.2 Other means of identification

Product number -
Other names diethyl cyano(methoxymethyl)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:59463-48-8 SDS

59463-48-8Relevant academic research and scientific papers

Photocatalytic Alkylation of Pyrroles and Indoles with α-Diazo Esters

Ciszewski, Lukasz W.,Durka, Jakub,Gryko, Dorota

, p. 7028 - 7032 (2019)

This article describes the photoalkylation of electron-rich aromatic compounds with diazo esters. C-2-alkylated indoles and pyrroles are obtained with good yields even though the photocatalyst loading is as low as 0.075 mol %. For EWG-substituted substrates, the addition of a catalytic amount of N,N-dimethyl-4-methoxyaniline is required. Both EWG-EWG- and EWG-EDG-substituted diazo esters are suitable as alkylating agents. The reaction selectivity and mechanistic experiments suggest that carbenes/carbenoid intermediates are not involved in the reaction pathway.

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