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Phosphinic acid, phenyl(trichloromethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54944-19-3

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54944-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54944-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,4 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54944-19:
(7*5)+(6*4)+(5*9)+(4*4)+(3*4)+(2*1)+(1*9)=143
143 % 10 = 3
So 54944-19-3 is a valid CAS Registry Number.

54944-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [ethoxy(trichloromethyl)phosphoryl]benzene

1.2 Other means of identification

Product number -
Other names Phenyl-trichlormethyl-phosphinsaeure-aethylester

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:54944-19-3 SDS

54944-19-3Relevant academic research and scientific papers

Preparation of alkyl- and aryl-aminomethylphosphinic acids

Berte-Verrando, Sylvie,Nief, Francois,Patois, Carl,Savignac, Philippe

, p. 2045 - 2048 (1995)

Diethyl chloromethylphosphonate upon successive treatment with POCl3 and Grignard reagents (RMgX) gave alkyl(chloromethyl)phosphinates.Phenyl(chloromethyl)phosphinate was prepared by deuterolysis of the α-silylated α-phosphonylated ca

New syntheses of 1-chloroalkylphosphinates

Morise, Xavier,Savignac, Philippe,Denis, Jean-Marc

, p. 2179 - 2185 (2007/10/03)

Different approaches to the synthesis of 1-chloroalkylphosphinates are described. Initially, we tried to extend a reaction described by Kabachnik for the preparation of chloromethylphosphinic acid chlorides [R1(Cl)P(O)CH2Cl] to C-substituted derivatives. We also considered the possibility of synthesizing the title compounds by routes already described for the formation of diethyl 1-chloroalkylphosphonates. Although these methods have allowed us to obtain several of the desired phosphinates, they suffer from limitations that restrict their synthetic applications. Finally, we have developed a more general approach that allows the formation of a wide range of phosphinates. It involves a selective P-C bond formation by reaction of MeMgCl and PhMgCl with phosphonochloridates, which are prepared by P-chlorination of 1-chloroalkylphosphonates.

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