89891-38-3 Usage
Uses
Used in Chemical Synthesis:
(3,5-Dichlorophenyl)phosphonic acid is used as a precursor in the synthesis of other organic phosphonic acids for various applications due to its reactive functional groups and ability to form stable derivatives.
Used in Flame Retardants Industry:
(3,5-Dichlorophenyl)phosphonic acid is used as a key component in the development of flame retardants to enhance the fire resistance of materials, providing safety and protection in various products.
Used in Agrochemicals:
(3,5-Dichlorophenyl)phosphonic acid is used as an active ingredient in the production of herbicides and fungicides to control the growth of unwanted plants and fungi, ensuring better crop yields and protection of agricultural products.
Used in Pharmaceutical Industry:
(3,5-Dichlorophenyl)phosphonic acid is used as an intermediate in the synthesis of specific pharmaceuticals, contributing to the development of new drugs and therapeutic agents for various medical conditions.
Due to its broad range of applications, (3,5-Dichlorophenyl)phosphonic acid is of significant interest to researchers and industries in various fields, making it a valuable compound for further exploration and development.
Check Digit Verification of cas no
The CAS Registry Mumber 89891-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,9 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89891-38:
(7*8)+(6*9)+(5*8)+(4*9)+(3*1)+(2*3)+(1*8)=203
203 % 10 = 3
So 89891-38-3 is a valid CAS Registry Number.
89891-38-3Relevant academic research and scientific papers
(Benzene-1,3,5-triyl)tris[phosphine] (C6H3(PH2)3) and (benzene-1,3,5-triyl)tris[phosphonic acid] (C6H3[P(O)(OH)2]3). Absence of hydrogen bonding in solid primary phosp
Reiter, Stephan A.,Assmann, Bernd,Nogai, Stefan D.,Mitzel, Norbert W.,Schmidbaur, Hubert
, p. 1140 - 1150 (2007/10/03)
The prolonged photo-Arbuzov reaction (3 weeks, Hg lamp) of 1,3,5-trichloro-benzene with a large excess of trimethyl phosphite (as a solvent) at 50° gives moderate yields of dimethyl (3,5-dichlorophenyl)phosphonate (1; 14.5%), tetramethyl (5-chloro-1,3-phe
