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diethyl (4-fluorophenyl)phosphoramidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50672-18-9

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50672-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50672-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,7 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50672-18:
(7*5)+(6*0)+(5*6)+(4*7)+(3*2)+(2*1)+(1*8)=109
109 % 10 = 9
So 50672-18-9 is a valid CAS Registry Number.

50672-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-diethoxyphosphoryl-4-fluoroaniline

1.2 Other means of identification

Product number -
Other names diethyl(4-fluorophenyl)phosphoramidate

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:50672-18-9 SDS

50672-18-9Relevant academic research and scientific papers

Reinvestigation of the iodine-mediated phosphoramidation reaction of amines and P(OR)3 and its synthetic applications

Chen, Xunwei,Xiao, Zecai,Chu, Hanyu,Wang, Bo,Peng, Ai-Yun

, p. 6783 - 6790 (2018/09/29)

A systematic study on the iodine-mediated phosphoramidation reaction of amines and trialkyl phosphites was conducted, which not only disclosed the factors affecting the reaction but also revealed that it could proceed smoothly in CH2Cl2 at room temperature in open air. Using this method, various phosphoramidates with different aliphatic amines and aromatic amines were synthesized in good to excellent yields. Our present investigation shows that this underused method is actually a mild, practical and general way to synthesize phosphoramidates and will have wide applications.

Organophotocatalytic Synthesis of Phosphoramidates

Meazza, Marta,Kowalczuk, Agnieszka,Shirley, Luke,Yang, Jung Woon,Guo, Hao,Rios, Ramon

, p. 719 - 723 (2016/03/09)

We describe the use of visible light in conjunction with an organic dye for the synthesis of phosphoramidates. Cross dehydrogenative coupling reactions between phosphites and amines are reported using organic dyes and light as catalysts for the first time. It is not only a novel application of organic dyes but also fulfils the requirement of sustainability and green chemistry avoiding the use of chromatographic purification techniques. The product was simply isolated from the reaction mixture via an acid-base work-up procedure, rendering the pure product in good yields.

Iodine catalyzed solvent-free cross-dehydrogenative coupling of arylamines and H-phosphonates for the synthesis of N-arylphosphoramidates under atmospheric conditions

Dar, Bashir Ahmad,Dangroo, Nisar A.,Gupta, Amit,Wali, Aarti,Khuroo, Mohammad Akbar,Vishwakarma, Ram A.,Singh, Baldev

, p. 1544 - 1548 (2014/03/21)

Aerobic oxidative coupling of various arylamines and H-phosphonates to the corresponding N-arylphosphoramidates has been achieved under solvent-free conditions using molecular iodine. This protocol works at room temperature furnishing the corresponding P-

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