Welcome to LookChem.com Sign In|Join Free
  • or
Dimethyl(3-Methoxybenzyl)phosphonate, 98 % is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135203-54-2

Post Buying Request

135203-54-2 Suppliers

Recommended suppliers

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

135203-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135203-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,0 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 135203-54:
(8*1)+(7*3)+(6*5)+(5*2)+(4*0)+(3*3)+(2*5)+(1*4)=92
92 % 10 = 2
So 135203-54-2 is a valid CAS Registry Number.

135203-54-2SDS

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-(dimethoxyphosphorylmethyl)-3-methoxybenzene

1.2 Other means of identification

Product number -
Other names Dimethyl(3-Methoxybenzyl)phosphonate

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:135203-54-2 SDS

135203-54-2Relevant academic research and scientific papers

Palladium-catalyzed benzylic substitution of benzyl carbonates with phosphorus nucleophiles

Makida, Yusuke,Usui, Kazumi,Ueno, Satoshi,Kuwano, Ryoichi

, p. 1814 - 1817 (2017/11/23)

A wide range of benzyl carbonates reacted with dimethyl phosphonate or diphenylphosphine oxide in the presence of the palladium catalyst, [Pd(η3-allyl)Cl]2DPEphos, to give dimethyl benzylphosphonates and benzyldiphenylphosphine oxides in high yields. The catalytic phosphonylation was applied to the one-pot synthesis of alkenes from the benzyl esters.

Palladium(II)-catalyzed ortho-arylation of benzylic phosphonic monoesters using potassium aryltrifluoroborates

Meng, Xiangjian,Kim, Sunggak

, p. 11247 - 11254 (2013/12/04)

The new monophosphonic acid directing group was successfully utilized in the Pd (II)-catalyzed ortho-arylation of benzylic phosphonic monoesters using potassium aryltrifluoroborates. A wide range of benzylic phosphonic monoesters underwent clean ortho-ary

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 135203-54-2