1250397-29-5 Usage
Description
(2,6-Difluorophenyl)phosphonic acid diethyl ester is a chemical compound with the chemical formula C10H13F2O3P. It is a diethyl ester derivative of (2,6-difluorophenyl)phosphonic acid and is typically used as an intermediate in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
(2,6-Difluorophenyl)phosphonic acid diethyl ester is used as a building block for the production of pharmaceutical drugs. It plays a crucial role in the synthesis of various drug molecules, contributing to the development of new medications for various diseases and conditions.
Used in Agrochemical Industry:
(2,6-Difluorophenyl)phosphonic acid diethyl ester is used as a building block for the production of insecticides and herbicides. It helps in the development of effective pest control agents that protect crops and enhance agricultural productivity.
Used as an Intermediate in Organic Synthesis:
(2,6-Difluorophenyl)phosphonic acid diethyl ester is used as an intermediate in the synthesis of various organic compounds. Its unique chemical structure allows it to be a versatile building block in the creation of a wide range of chemical products, including specialty chemicals and materials for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1250397-29-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,0,3,9 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1250397-29:
(9*1)+(8*2)+(7*5)+(6*0)+(5*3)+(4*9)+(3*7)+(2*2)+(1*9)=145
145 % 10 = 5
So 1250397-29-5 is a valid CAS Registry Number.
1250397-29-5Relevant articles and documents
Cobalt catalyzed C-P bond formation by cross-coupling of boronic acids with P(O)H compounds in presence of zinc
Hicks, Ian,McTague, Jonathan,Hapatsha, Tatiana,Teriak, Rania,Kaur, Parminder
, (2020/01/31)
In our current work, we have reported the first cobalt-catalyzed cross-coupling of arylboronic acid with alkyl/aryl phosphites under mild conditions. The reaction was carried out in the presence of zinc powder as an additive and ter-pyridine as a ligand. The use of non-precious cobalt salt makes the protocol advantageous, as it is inexpensive and more abundant than the previously used methods where precious metal salts (Pd and Pt) were used. The reaction has a wide substrate scope and the products were obtained in good yields.
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
