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Phosphonic acid, (4-chlorophenyl)-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13114-07-3

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13114-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13114-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13114-07:
(7*1)+(6*3)+(5*1)+(4*1)+(3*4)+(2*0)+(1*7)=53
53 % 10 = 3
So 13114-07-3 is a valid CAS Registry Number.

13114-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-dimethoxyphosphorylbenzene

1.2 Other means of identification

Product number -
Other names 4-Chlor-phenylphosphonsaeure-dimethylester

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:13114-07-3 SDS

13114-07-3Relevant academic research and scientific papers

C-P bond formation of cyclophanyl-, and aryl halides: Via a UV-induced photo Arbuzov reaction: A versatile portal to phosphonate-grafted scaffolds

Br?se, Stefan,Hassan, Zahid,Nieger, Martin,O?wald, Simon,Zippel, Christoph

, p. 3309 - 3312 (2022/02/11)

A new versatile method for the C-P bond formation of (hetero)aryl halides with trimethyl phosphite via a UV-induced photo-Arbuzov reaction, accessing diverse phosphonate-grafted arenes, heteroarenes and co-facially stacked cyclophanes under mild reaction

Cu2O/TiO2 nanoparticles as visible light photocatalysts concerning C(sp2)-P bond formation

Hosseini-Sarvari, Mona,Jafari, Fattaneh,Mohajeri, Afshan,Hassani, Nasim

, p. 4044 - 4051 (2018/08/24)

A novel and efficient method has been developed for the construction of an aromatic-phosphorus (Ar-P) bond under visible light irradiation using Cu2O/TiO2 nanoparticles as inexpensive and available photocatalysts. This protocol is a simple system without the use of any base, ligand, oxidant, or special conditions. This is the first report for the synthesis of arylphosphonates from arylhydrazines in visible light irradiation.

Copper-catalyzed coupling reaction of arylhydrazines and trialkylphosphites

Chen, Sheng-Yan,Zeng, Run-Sheng,Zou, Jian-Ping,Asekun, Olayinka Taiwo

, p. 1449 - 1453 (2014/03/21)

A novel CuO-catalyzed coupling reaction of arylhydrazines with trialkyl phosphites to afford arylphosphonates is described. The reaction proceeded at 80 C in air without external reductants, oxidants, and ligands.

A facile route to vinyl- and arylphosphonates by vinyl and aryl radical trapping with (MeO)3P

Jiao, Xian-Yun,Bentrude, Wesley G.

, p. 3303 - 3306 (2007/10/03)

The generation of vinyl or aryl radicals under classical, thermal AIBN/n-Bu3SnH conditions at 80 °C in the presence of an excess of (MeO)3P gives rise to the corresponding vinyl- or arylphosphonates in good yields. This approach comp

Palladium-Catalyzed Phase-Transfer Arylation of Dialkyl Phosphonates

Kabachnik,Solntseva,Izmer,Novikova,Beletskaya

, p. 93 - 97 (2007/10/03)

Palladium-catalyzed phase-transfer arylation of dialkyl phosphonates with various iodo- and bromoarenes has been studied. The arylation has also been effected in the absence of ligand. A simple preparative procedure for synthesizing arylphosphonic acids has been developed.

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