Welcome to LookChem.com Sign In|Join Free
  • or
DIETHYL(4-NITROPHENYL)PHOSPHONATE, with the chemical formula C10H13NO5P, is a phosphonate ester that serves as a versatile reagent in organic synthesis. This colorless to pale yellow liquid, characterized by a faint odor, is recognized for its selective inhibitory action on acetylcholinesterase, a key enzyme in neurotransmitter signaling. This property renders it a significant entity in the research of neurodegenerative diseases, such as Alzheimer's, and in the development of potential therapeutics. Moreover, its capacity to facilitate diverse chemical reactions makes it valuable in the synthesis of pharmaceuticals and agrochemicals. However, due to its toxic nature, it requires careful handling to prevent harmful effects from ingestion, inhalation, or skin contact.

1754-42-3

Post Buying Request

1754-42-3 Suppliers

Recommended suppliers

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

1754-42-3 Usage

Uses

Used in Pharmaceutical Research:
DIETHYL(4-NITROPHENYL)PHOSPHONATE is used as a research tool for studying neurotransmitter signaling due to its selective inhibition of acetylcholinesterase, which aids in understanding the mechanisms of neurodegenerative diseases like Alzheimer's.
Used in Drug Synthesis:
In the pharmaceutical industry, DIETHYL(4-NITROPHENYL)PHOSPHONATE is used as a synthetic intermediate for the development of various drugs, leveraging its ability to mediate a range of chemical reactions essential in drug formulation.
Used in Agrochemical Development:
Similarly, in the agrochemical sector, DIETHYL(4-NITROPHENYL)PHOSPHONATE is utilized as a reagent in the synthesis of agrochemicals, contributing to the creation of effective products for agricultural applications.
Used in Organic Synthesis:
DIETHYL(4-NITROPHENYL)PHOSPHONATE is used as a reagent in organic synthesis for its capacity to participate in multiple reaction types, making it a valuable component in the preparation of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1754-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1754-42:
(6*1)+(5*7)+(4*5)+(3*4)+(2*4)+(1*2)=83
83 % 10 = 3
So 1754-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14NO5P/c1-3-15-17(14,16-4-2)10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3

1754-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-diethoxyphosphoryl-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names para-nitro-phenylphosphonate diethylique

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:1754-42-3 SDS

1754-42-3Relevant academic research and scientific papers

Electrochemical phosphorylation of arenes catalyzed by cobalt under oxidative and reductive conditions

Strekalova,Grinenko,Gryaznova,Kononov,Dolengovski,Budnikova

, p. 506 - 509 (2019)

Catalyst capable to operate in cathode and anode spaces simultaneously was found. Electrochemical regeneration of active form of catalyst Co2+bpy (1%) under oxidative as well as reductive conditions allows the C–H/P–H coupling of dialkyl-H-phos

Palladium anchored on a covalent organic framework as a heterogeneous catalyst for phosphorylation of aryl bromides

Chen, Yu-Xuan,Zhang, Shuo,Xue, Yu-Jie,Mo, Li-Ping,Zhang, Zhan-Hui

, (2021/11/05)

A simple azine-linked covalent organic framework (COF) with high thermal and chemical stabilities has been prepared by using deep eutectic solvent (DES) as green media. The as-synthesized COF was employed as heterogeneous ligand for immobilization of PdII. The obtained Pd-supported COF nanoparticles catalyst (defined as Pd/TFPT-Azine-COF) was found to be an efficient heterogeneous catalyst for the Hirao reaction of aryl halides and dialkyl phosphites or diphenylphosphine oxide with excellent recyclability, reusability, and retention of crystallinity.

STRAD-BINDING AGENTS AND USES THEREOF

-

Paragraph 0956-0958, (2021/08/06)

Disclosed herein, inter alia, are compounds for binding STRAD pseudokinase and uses thereof.

Discovery of STAT3 and Histone Deacetylase (HDAC) Dual-Pathway Inhibitors for the Treatment of Solid Cancer

Ren, Yuhao,Li, Shanshan,Zhu, Ren,Wan, Chengying,Song, Dongmei,Zhu, Jiawen,Cai, Guiping,Long, Sihui,Kong, Lingyi,Yu, Wenying

, p. 7468 - 7482 (2021/06/28)

Nowadays, simultaneous inhibition of multiple targets through drug combination is an important anticancer strategy owing to the complex mechanism behind tumorigenesis. Recent studies have demonstrated that the inhibition of histone deacetylases (HDACs) will lead to compensated activation of a notorious cancer-related drug target, signal transducer and activator of transcription 3 (STAT3), in breast cancer through a cascade, which probably limits the anti-proliferation effect of HDAC inhibitors in solid tumors. By incorporating the pharmacophore of the HDAC inhibitor SAHA (vorinostat) into the STAT3 inhibitor pterostilbene, a series of potent pterostilbene hydroxamic acid derivatives with dual-target inhibition activity were synthesized. An excellent hydroxamate derivate, compound 14, inhibited STAT3 (KD = 33 nM) and HDAC (IC50 = 23.15 nM) with robust potency in vitro. Compound 14 also showed potent anti-proliferation ability in vivo and in vitro. Our study provides the first STAT3 and HDAC dual-target inhibitor for further exploration.

Visible-light-mediated phosphonylation reaction: formation of phosphonates from alkyl/arylhydrazines and trialkylphosphites using zinc phthalocyanine

Hosseini-Sarvari, Mona,Koohgard, Mehdi

, p. 5905 - 5911 (2021/07/12)

In this work, we developed a ligand- and base-free visible-light-mediated protocol for the photoredox syntheses of arylphosphonates and, for the first time, alkyl phosphonates. Zinc phthalocyanine-photocatalyzed Csp2-P and Csp3-P bond formations were efficiently achieved by reacting aryl/alkylhydrazines with trialkylphosphites in the presence of air serving as an abundant oxidant. The reaction conditions tolerated a wide variety of functional groups.

Fe-MIL-101 modified by isatin-Schiff-base-Co: a heterogeneous catalyst for C-C, C-O, C-N, and C-P cross coupling reactions

Farrokhi, Alireza,Rouzifar, Majid,Sansano, José Miguel,Sobhani, Sara

, p. 19963 - 19976 (2021/11/12)

A metal-organic framework functionalized with a cobalt-complex is preparedviapost-synthetic modification of Fe-MIL-101-NH2. Initially, Fe-MIL-101-NH2reacted with isatin to produce Fe-MIL-101-isatin-Schiff-base, which can anchor the cobalt by the addition of cobalt acetate. The resulting MOF-Co catalyst is characterized by employing multiple techniques. This new modified MOF acts as a heterogeneous and recyclable catalyst for efficient Ullmann, Buchwald-Hartwig, Hirao, Hiyama and Mizoroki-Heck cross-coupling reactions of several aryl halides/phenylboronic acid/phenyltosylate with phenols, anilines/heterocyclic amines, triethyl phosphite, triethoxyphenylsilane and alkenes and generates the expected coupling products in good to high yields.

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.

A hydrophilic heterogeneous cobalt catalyst for fluoride-free Hiyama, Suzuki, Heck and Hirao cross-coupling reactions in water

Sobhani, Sara,Hosseini Moghadam, Hadis,Skibsted, J?rgen,Sansano, José Miguel

, p. 1353 - 1365 (2020/03/11)

A hydrophilic heterogeneous cobalt catalyst of chitosan, denoted as mTEG-CS-Co-Schiff-base, has been successfully prepared. This newly synthesized catalyst was characterized by different methods such as XRD, FE-SEM, TEM, TGA, FT-IR, 13C{1H} CP/MAS NMR, XPS and ICP analyses. The catalyst displayed excellent activity for the palladium and fluoride-free Hiyama, Suzuki, Heck and Hirao reactions of various aryl iodides, bromides and chlorides (i.e., the most challenging aryl halides which are cheaper and more widely available than aryl iodides and bromides) in water. The presence of triethylene glycol tags with hydrophilic character on the Co-complex supported on chitosan provides dispersion of the catalyst particles in water, which leads to higher catalytic performance and also facile catalyst recovery by successive extraction. It was reused for at least six successive runs without any discernible decrease in its catalytic activity or any remarkable changes in catalyst structure. The use of water as a green solvent, without requiring any additive or organic solvent, as well as use of a low cost and abundant cobalt catalyst instead of expensive Pd catalysts along with the catalyst recovery and scalability, make this method favorable from environmental and economic points of view for the C-C and C(sp2)-P coupling reactions. Notably, this is the first report on the application of a cobalt catalyst in Hiyama reactions.

C-P bond construction catalyzed by NiII immobilized on aminated Fe3O4@TiO2 yolk-shell NPs functionalized by (3-glycidyloxypropyl)trimethoxysilane (Fe3O4@TiO2 YS-GLYMO-UNNiII

Ghasemzadeh, Maryam Sadat,Akhlaghinia, Batool

, p. 5341 - 5356 (2019/04/05)

NiII immobilized on aminated Fe3O4@TiO2 yolk-shell NPs functionalized by (3-glycidyloxypropyl)trimethoxysilane (Fe3O4@TiO2 YS-GLYMO-UNNiII) was prepared as a stable, h

Direct Aryloxylation/Alkyloxylation of Dialkyl Phosphonates for the Synthesis of Mixed Phosphonates

Huang, Hai,Denne, Johanna,Yang, Chou-Hsun,Wang, Haobin,Kang, Jun Yong

supporting information, p. 6624 - 6628 (2018/05/14)

A strategy for the direct functionalization strategy of inertial dialkyl phosphonates with hydroxy compounds to afford diverse mixed phosphonates with good yields and functional-group tolerance has been developed. Mechanistic investigations involving both NMR studies and DFT studies suggest that an unprecedented highly reactive PV species (phosphoryl pyridin-1-ium salt), a key intermediate for this new synthetic transformation, is generated in situ from dialkyl phosphonate in the presence of Tf2O/pyridine.

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 1754-42-3