5055-14-1 Usage
Description
(2-bromoethyl)(diphenyl)phosphane oxide is an organophosphorus compound with the molecular formula C14H14BrOP. It features a bromoethyl group and a diphenylphosphane oxide group, making it a versatile reagent in chemical synthesis.
Uses
Used in Organic Synthesis:
(2-bromoethyl)(diphenyl)phosphane oxide is used as a reagent for the preparation of various phosphorus-containing compounds, contributing to the development of new chemical entities and materials.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-bromoethyl)(diphenyl)phosphane oxide serves as a building block for the synthesis of bioactive compounds, potentially leading to the discovery of new pharmaceuticals and therapeutic agents.
Used in Chemical Research:
(2-bromoethyl)(diphenyl)phosphane oxide is utilized in research laboratories for studying the properties and reactions of organophosphorus compounds, furthering scientific understanding and innovation in chemistry.
It is crucial to handle (2-bromoethyl)(diphenyl)phosphane oxide with care due to its potentially hazardous nature, as it may cause irritation and damage to the skin, eyes, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 5055-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,5 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5055-14:
(6*5)+(5*0)+(4*5)+(3*5)+(2*1)+(1*4)=71
71 % 10 = 1
So 5055-14-1 is a valid CAS Registry Number.
5055-14-1Relevant articles and documents
ω-haloalkylphosphoryl compounds: Synthesis and properties
Ragulin
, p. 1928 - 1937 (2013/06/05)
A general method of the synthesis of ω-haloalkylphosphoryl compounds was developed, a series of compounds of phosphonic and phosphine oxide type were synthesized. The ability of some ω-haloalkylphosphonates to undergo intramolecular cyclization into the corresponding 1,2-oxaphospholane and 1,2-oxaphosphorine was investigated depending on the solvent polarity, the presence of halogen ions in the solution, and temperature. Tetrahydrofuran was chosen as one of the most suitable solvents for the alkylation of CH acids with ω-haloalkylphosphoryl compounds.
