28482-01-1 Usage
Description
(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.
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.
28482-01-1Relevant articles and documents
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
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
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.
