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(2-bromoethyl)phosphonic dichloride is a colorless liquid chemical compound with the formula C2H4BrCl2OP. It is known for its high reactivity and versatility, making it a significant compound in organic chemistry.

28482-01-1

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28482-01-1 Usage

Uses

Used in Flame Retardant Production:
(2-bromoethyl)phosphonic dichloride is used as an intermediate in the production of flame retardants, which are essential for enhancing the fire resistance of various materials.
Used in Water Treatment Chemicals:
In the water treatment industry, (2-bromoethyl)phosphonic dichloride serves as a precursor for developing chemicals that help in purifying water and maintaining water quality.
Used in Agrochemicals:
(2-bromoethyl)phosphonic dichloride is utilized as a component in the synthesis of agrochemicals, contributing to the development of products that protect crops and enhance agricultural productivity.
Used in Pharmaceutical Industry:
(2-bromoethyl)phosphonic dichloride is employed as a building block in the pharmaceutical sector for the development of potential drug candidates, highlighting its importance in creating new medicines.

Check Digit Verification of cas no

The CAS Registry Mumber 28482-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,8 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28482-01:
(7*2)+(6*8)+(5*4)+(4*8)+(3*2)+(2*0)+(1*1)=121
121 % 10 = 1
So 28482-01-1 is a valid CAS Registry Number.

28482-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-dichlorophosphorylethane

1.2 Other means of identification

Product number -
Other names Bromethanphosphonsaeurechlorid

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:28482-01-1 SDS

28482-01-1Relevant academic research and scientific papers

The synthesis of methylated, phosphorylated, and phosphonated 3′-aminoacyl-tRNASec mimics

Rigger, Lukas,Schmidt, Rachel L.,Holman, Kaitlyn M.,Simonovic, Miljan,Micura, Ronald

supporting information, p. 15872 - 15878 (2014/04/03)

The twenty first amino acid, selenocysteine (Sec), is the only amino acid that is synthesized on its cognate transfer RNA (tRNASec) in all domains of life. The multistep pathway involves O-phosphoseryl-tRNA: selenocysteinyl-tRNA synthase (SepSe

Reaction of dibromoalkanes with silyl phosphites. Synthesis and properties of mono-and diphosphonoalkanes

Pudovik,Terent'eva,Kibardina,Pudovik

, p. 714 - 719 (2008/02/02)

Reactions of dibromoethane and dibromopropane with silyl phosphites are studied. Mono-and diphosphonoalkanes of various structures were prepared, and their chemical properties were studied. Pleiades Publishing, Inc., 2006.

Experimental and theoretical investigation of intramolecular transformations of silicon-containing (haloalkyl)phosphorylated ureas and acylamides

Pudovik,Chmutova,Kibardina,Terent'eva,Bagautdinova,Khailova,Kamalov,Pudovik

, p. 376 - 380 (2008/02/05)

Silicon-containing chloromethylphosphorylated ureas undergo transformation involving evolution of chlorotrimethylsilane and formation of 1,3,4-oxazaphospholes. Their analogs, silicon-containing phosphorylated acylamides, transform in another way, viz. by

Cationic phosphonolipids containing quaternary phosphonium and arsonium groups for DNA transfection with good efficiency and low cellular toxicity

Guenin, Erwann,Herve, Anne-Cecile,Floch, Virginie,Loisel, Severine,Yaouanc, Jean-Jacques,Clement, Jean-Claude,Ferec, Claude,Des Abbayes, Herve

, p. 629 - 631 (2007/10/03)

Replacing the ammonium polar head in cationic lipids 1 (A = N) by a phosphonium or an arsonium group (A=P, As) improves their properties as synthetic vectors for DNA transfection. The increased volume of the cationic head is supposed to modify the interactions of the vector with the solvent and DNA.

A NEW AND VERSATILE PHOSPHONYLATION APPROACH

Klein, P.A.M. van der,Dreef, C.E.,Marel, G.A. van der,Boom, J.H. van

, p. 5473 - 5476 (2007/10/02)

The bifunctional reagent bis(benzotriazolyl)-2-bromoethylphosphonate has been used successfully for the preparation of 2-amino-, 2-N-methylamino- and 2-N-dimethylaminoethylphosphonates of methyl 2,3,4-tri-O-benzoyl-β-D-galactopyranoside.

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