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

10419-80-4

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10419-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10419-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,1 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10419-80:
(7*1)+(6*0)+(5*4)+(4*1)+(3*9)+(2*8)+(1*0)=74
74 % 10 = 4
So 10419-80-4 is a valid CAS Registry Number.

10419-80-4 Well-known Company Product Price

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  • TCI America

  • (D5095)  Diethyl (Ethoxymethyl)phosphonate  >98.0%(GC)

  • 10419-80-4

  • 5g

  • 990.00CNY

  • Detail
  • TCI America

  • (D5095)  Diethyl (Ethoxymethyl)phosphonate  >98.0%(GC)

  • 10419-80-4

  • 25g

  • 3,650.00CNY

  • Detail

10419-80-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(diethoxyphosphorylmethoxy)ethane

1.2 Other means of identification

Product number -
Other names Aethoxymethyl-phosphonsaeure-diaethylester

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:10419-80-4 SDS

10419-80-4Relevant academic research and scientific papers

An improved synthesis of adefovir and related analogues

Jones, David J.,O’Leary, Eileen M.,O’Sullivan, Timothy P.

supporting information, p. 801 - 810 (2019/04/17)

An improved synthesis of the antiviral drug adefovir is presented. Problems associated with current routes to adefovir include capricious yields and a reliance on problematic reagents and solvents, such as magnesium tert-butoxide and DMF, to achieve high conversions to the target. A systematic study within our laboratory led to the identification of an iodide reagent which affords higher yields than previous approaches and allows for reactions to be conducted up to 10 g in scale under milder conditions. The use of a novel tetrabutylammonium salt of adenine facilitates alkylations in solvents other than DMF. Additionally, we have investigated how regioselectivity is affected by the substitution pattern of the nucleobase. Finally, this chemistry was successfully applied to the synthesis of several new adefovir analogues, highlighting the versatility of our approach.

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