349-87-1 Usage
Description
(4-FLUORO-PHENYL)-PHOSPHONIC ACID, with the molecular formula C6H6FO3P, is a phosphonic acid derivative featuring a fluorine atom attached to a phenyl ring. This chemical compound is recognized for its utility as a building block in organic synthesis and holds potential in various fields, including pharmaceuticals, agrochemicals, material science, and as a catalyst in chemical reactions. Its unique properties in metal complexation when serving as a ligand in coordination chemistry further contribute to its diverse applications.
Uses
Used in Pharmaceutical and Agrochemical Industries:
(4-FLUORO-PHENYL)-PHOSPHONIC ACID is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its structural properties allow for the creation of a wide range of molecules with specific therapeutic or pesticidal effects.
Used in Material Science:
In the field of material science, (4-FLUORO-PHENYL)-PHOSPHONIC ACID is utilized for its potential to enhance or modify the properties of materials, such as improving their stability, reactivity, or other characteristics, depending on the specific application.
Used as a Catalyst in Chemical Reactions:
(4-FLUORO-PHENYL)-PHOSPHONIC ACID serves as a catalyst in various chemical reactions, facilitating and accelerating the process while remaining unchanged at the end of the reaction. Its unique properties enable it to be employed in different types of reactions, enhancing the efficiency and selectivity of the process.
Used in Coordination Chemistry as a Ligand:
(4-FLUORO-PHENYL)-PHOSPHONIC ACID exhibits unique properties when used as a ligand in coordination chemistry, playing a crucial role in the formation of metal complexes. Its ability to bind with metal ions can lead to the development of new compounds with specific properties and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 349-87-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 349-87:
(5*3)+(4*4)+(3*9)+(2*8)+(1*7)=81
81 % 10 = 1
So 349-87-1 is a valid CAS Registry Number.
349-87-1Relevant articles and documents
Synthesis, characterization and properties of titanium phosphonate clusters
Hayami, Ryohei,Sagawa, Takuya,Tsukada, Satoru,Yamamoto, Kazuki,Gunji, Takahiro
, p. 1 - 8 (2018/04/02)
Titanium phosphonate clusters were synthesized by the reactions of titanium tetraisopropoxide (Ti(OiPr)4) with arylphosphonic acids (ArPO3H2, Ar = Ph, 1-Nap, 4-MeOPh, 4-FPh, 4-ClPh, 4-BrPh, and 4-BrBn) and H2O in tetrahydrofuran (THF) at room temperature. [Ti4(μ3-O)(OiPr)5(μ-OiPr)3(O3PAr)3]·solv (Ar = Ph (1), 1-Nap (2), 4-MeOPh (3), 4-FPh (4), 4-ClPh (5); solv = thf for 1 and 2 or 2-propanol for 3–5) were isolated as new Ti4P3-type clusters, while Ti7(μ3-O)2(OiPr)6(μ-OiPr)6(O3PBnBr)6 (6) was isolated as a Ti7P6-type cluster. A co-crystal of Ti4P3- (7a) and Ti7P6-type (7b) clusters were obtained when 4-BrPhPO3H2 was used, and [Ti(OiPr)(acac)(O3PPh)]4 (8), a new cage cluster, was obtained when Ti(acac)2(OiPr)2 (Hacac = acetylacetone) was reacted with PhPO3H2.
Synthesis and proton dissociation properties of arylphosphonates: A microwave-assisted catalytic arbuzov reaction with aryl bromides
Keglevich, Gyoergy,Gruen, Alajos,Boelcskei, Adrienn,Drahos, Laszlo,Kraszni, Marta,Balogh, Gyoergy T.
, p. 574 - 582 (2013/01/15)
A series of substituted diethyl arylphosphonates was synthesized by the microwave-assisted Arbuzov reaction of triethyl phosphite and aryl bromides in the presence of NiCl2 as the catalyst under solvent-free conditions in good yields. The resulting phosphonates were hydrolyzed to the corresponding arylphosphonic acids whose acidity was evaluated by physicochemical methods.
ELECTRONIC DEVICES COMPRISING NOVEL PHOSPHONIC ACID SURFACE MODIFIERS
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Page/Page column 22, (2010/11/03)
In some embodiments, the inventions described herein relate to a composition of matter comprising a molecule having the structure: wherein: independently at each occurrence, R1 is a halogen, a alkyl group, a heteroalkyl group, an aryl group, or a heteroaryl group; R2 comprises from 3 to 30 CH2- groups, n = 0-5, m = 0-5, q = 1-3, and R2 comprises at least one ether linkage
