1000-16-4 Usage
Uses
Used in Organic Synthesis:
Diethyl [(dibutylamino)methyl]phosphonate is used as an intermediate in the synthesis of various organic compounds, contributing to the formation of complex molecular structures and facilitating chemical reactions.
Used in Metal Complexation:
As a ligand, diethyl [(dibutylamino)methyl]phosphonate is used in metal complexation to bind with metal ions, which is crucial for the development of catalysts and other coordination compounds.
Used in Polymer Production:
Diethyl [(dibutylamino)methyl]phosphonate is used as a stabilizer in polymer production, enhancing the properties and performance of the resulting polymers.
Used in Agricultural Products:
Diethyl [(dibutylamino)methyl]phosphonate is used in the manufacture of agricultural products, potentially contributing to the development of more effective and safer agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, diethyl [(dibutylamino)methyl]phosphonate is used in the development of new drugs, leveraging its unique chemical properties to create innovative therapeutic agents.
Used in Flame Retardants:
Diethyl [(dibutylamino)methyl]phosphonate is utilized in the production of flame retardants, helping to improve the fire safety of various materials and products.
It is important to handle diethyl [(dibutylamino)methyl]phosphonate with care due to its potential hazards and toxic effects, ensuring safe practices in its application across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1000-16-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1000-16:
(6*1)+(5*0)+(4*0)+(3*0)+(2*1)+(1*6)=14
14 % 10 = 4
So 1000-16-4 is a valid CAS Registry Number.
1000-16-4Relevant academic research and scientific papers
Catalyst-Free and Selective C-N Bond Functionalization: Stereospecific Three-Component Coupling of Amines, Dichloromethane, and >P(O)H Species Affording α-Aminophosphorus Compounds
Zhao, Yalei,Chen, Xiuling,Chen, Tieqiao,Zhou, Yongbo,Yin, Shuang-Feng,Han, Li-Biao
, p. 62 - 69 (2015/09/01)
Catalyst-free and selective C-N bond functionalization has been achieved through three-component coupling of amines, dihalomethane, and >P(O)H species. This reaction takes place stereospecifically with retention of configuration at phosphorus, which can produce various new optically active phosphorus analogues of α-amino acids.
