Welcome to LookChem.com Sign In|Join Free

CAS

  • or

15754-51-5

Post Buying Request

15754-51-5 Suppliers

Recommended suppliersmore

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

15754-51-5 Usage

General Description

Bis(4-methoxyphenyl)phosphine oxide, also known as BMPO, is a chemical compound with the formula C14H15O3P. It is a phosphine oxide derivative that is commonly used as a photoinitiator in the polymer industry. BMPO is a highly efficient and versatile photoinitiator that is capable of initiating the polymerization of various monomers, such as acrylates and methacrylates, upon exposure to UV light. It is known for its excellent solubility in a wide range of organic solvents, and its ability to generate radicals under mild conditions, making it a popular choice for photopolymerization processes. Additionally, BMPO has been studied for its potential application in various fields, including dental materials, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 15754-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,5 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15754-51:
(7*1)+(6*5)+(5*7)+(4*5)+(3*4)+(2*5)+(1*1)=115
115 % 10 = 5
So 15754-51-5 is a valid CAS Registry Number.

15754-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-methoxyphenyl)-oxophosphanium

1.2 Other means of identification

Product number -
Other names bis(p-methoxyphenyl)phosphine oxide

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:15754-51-5 SDS

15754-51-5Relevant articles and documents

Electrochemical Oxidative C–H Phosphonylation of thiazole derivatives in ambient conditions

Li, Yang,Wu, Lei,Yang, Yan-Tong,Zhu, Jie,Zhu, Peng-Wei

, (2021/12/07)

We herein report a direct electrochemical dehydrogenative C–H phosphonylation of thiazoles derivatives with H2 evolution. Employing electricity as the green and sole oxidant, cheap metal as electrode, the anodic oxidation together with cathodic hydrogen evolution process provides a green and efficient strategy for C–H phosphonylation. A diverse range of phosphorus products were constructed under external metal and oxidant-free conditions at ambient temperature, featuring atom economy, simple operation and wide reaction scope.

Asymmetric Catalytic Approach to Multilayer 3D Chirality

Wu, Guanzhao,Liu, Yangxue,Rouh, Hossein,Ma, Liulei,Tang, Yao,Zhang, Sai,Zhou, Peng,Wang, Jia-Ying,Jin, Shengzhou,Unruh, Daniel,Surowiec, Kazimierz,Ma, Yanzhang,Li, Guigen

supporting information, p. 8013 - 8020 (2021/05/10)

The first asymmetric catalytic approach to multilayer 3D chirality has been achieved by using Suzuki-Miyaura cross-couplings. New chiral catalysts were designed and screened under various catalytic systems that proved chiral amide-phosphines to be more efficient ligands than other candidates. The multilayer 3D framework was unambiguously determined by X-ray structural analysis showing a parallel pattern of three layers consisting of top, middle and bottom aromatic rings. The X-ray structure of a catalyst complex, dichloride complex of Pd-phosphine amide, was obtained revealing an interesting asymmetric environment nearby the Pd metal center. Three rings of multilayer 3D products can be readily changed by varying aromatic ring-anchored starting materials. The resulting multilayer products displayed strong luminescence under UV irradiation and strong aggregation-induced emission (AIE). In the future, this work would benefit not only the field of asymmetric synthesis but also materials science, in particular polarized organic electronics, optoelectronics and photovoltaics.

Organic photoredox catalytic α-C(sp3)-H phosphorylation of saturated: Aza -heterocycles

Yi, Ming-Jun,Xiao, Teng-Fei,Li, Wen-Hui,Zhang, Yi-Fan,Yan, Pen-Ji,Zhang, Baoxin,Xu, Peng-Fei,Xu, Guo-Qiang

supporting information, p. 13158 - 13161 (2021/12/16)

A metal-free C(sp3)-H phosphorylation of saturated aza-heterocycles via the merger of organic photoredox and Br?nsted acid catalyses was established under mild conditions. This protocol provided straightforward and economic access to a variety of valuable α-phosphoryl cyclic amines by using commercially available diarylphosphine oxide reagents. In addition, the D-A fluorescent molecule DCQ was used for the first time as a photocatalyst and exhibited an excellent photoredox catalytic efficiency in this transformation. A series of mechanistic experiments and DFT calculations demonstrated that this transformation underwent a sequential visible light photoredox catalytic oxidation/nucleophilic addition process.

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

What can I do for you?
Get Best Price

Get Best Price for 15754-51-5