Welcome to LookChem.com Sign In|Join Free
  • or
Phosphonofluoridic acid, phenyl-, methyl ester, also known as Methyl phenylphosphonofluoridate, is a chemical compound with the molecular formula C7H8FO2P. It is a colorless, oily liquid that is soluble in organic solvents. Phosphonofluoridic acid, phenyl-, methyl ester is a derivative of phosphonofluoridic acid, where a phenyl group is attached to the phosphorus atom, and a methyl group is esterified to the hydroxyl group. Methyl phenylphosphonofluoridate is primarily used as a reagent in organic synthesis, particularly in the preparation of various phosphorus-containing compounds. It is also known for its potential use as a chemical warfare agent due to its ability to inhibit acetylcholinesterase, an enzyme essential for the proper functioning of the nervous system. However, it is important to note that the use of such compounds for warfare is prohibited under international law.

650-99-7

Post Buying Request

650-99-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

650-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 650-99-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 650-99:
(5*6)+(4*5)+(3*0)+(2*9)+(1*9)=77
77 % 10 = 7
So 650-99-7 is a valid CAS Registry Number.

650-99-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [fluoro(methoxy)phosphoryl]benzene

1.2 Other means of identification

Product number -
Other names Phosphonofluoridic acid,phenyl-,methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:650-99-7 SDS

650-99-7Relevant academic research and scientific papers

Phenylfluorophosphoranes: axial-equatorial fluorine exchange in RC6H4PF3H and intermolecular exchange in the PhPF2(H)OMe-MeOH-base system

Kruczynski, Leonard J.,Lemire, Alberta E.,Marat, Kirk,Janzen, Alexander F.

, p. 488 - 491 (2007/10/02)

Activation parameters for axial-equatorial fluorine exchange in arylfluorophophoranes PC6H4PF3H, where R = o-CF3, m-CF3, m-CH3, were studied by the dynamic nmr technique. Δ G298(excit.) varied between 53 and 56 kJ mol-1.The synthesis of difluoromethoxyphenylphosphorane, PhPF2(H)OMe, from PhPF2 and MeOH is catalyzed by small amounts of Et3N, pyridine, PhPF3H, or HF.Rapid intermolecular ligand exchange occurs in PhPF2(H)OMe after addition of methanol and a base such as triethylamine or pyridine.Under these conditions, exchange of fluorine, hydrogen, and methoxy ligands occurs, as shown by 1H, 19F, and 31P nmr.From a line shape analysis of the 31P nmr spectrum, the rate of P-F cleavage was found to be first order (1.17 +/- 0.2) in Et3N concentration, with Δ G(excit.)298 = 50 kJ mol-1 and Δ S (excit.) = -67 J mol-1 deg-1.An equilibrium constant of 1.8 at 25 deg C was found for the reaction of PhPF2(H)OMe with PhPF2.

Phosphorus-fluorine chemistry. XIII. The adduct of nitrosyl fluoride with phenyltetrafluorophosphorane. New fluorophosphates

Schmutzler,Reddy

, p. 191 - 197 (2007/10/04)

Nitrosyl fluoride was found to react with phenyltetrafluorophosphorane to form a solid, thermally unstable 1:1 adduct. Evidence for the formulation of this adduct as a nitrosyl salt, NO+C6H5PF5-, based on various chemical reactions, is presented. The novel fluoroanions, R(Ar)PF5-, together with alkyl(aryl)dialkylaminotrifluorophosphoranes, R(Ar)PF3NR2, are also obtained in the form of stable dialkylammonium salts upon dialkylaminolysis of tetrafluorophosphoranes, R(Ar)PF4. The stereochemistry of the R(Ar)PF5- anions, and of the alkyl(aryl)dialkylaminotrifluorophosphoranes, based on n.m.r. spectroscopic studies, is discussed. In contrast to nitrosyl fluoride, nitryl fluoride reacted with phenyltetrafluorophosphorane with direct nitration of the aromatic ring.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 650-99-7