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1,3,2-Benzodioxaphosphole, 4,6-bis(1,1-dimethylethyl)-2-methoxy-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146399-33-9

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146399-33-9 Usage

Chemical structure

1,3,2-Benzodioxaphosphole backbone with two tert-butyl groups and a methoxy group

Type of compound

Phosphole oxide derivative

Field of importance

Organic chemistry and materials science

Unique properties

Potential applications in catalysis, development of new materials with specific electronic and optical properties

Research focus

Exploration of its potential use as a ligand in coordination chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 146399-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,9 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 146399-33:
(8*1)+(7*4)+(6*6)+(5*3)+(4*9)+(3*9)+(2*3)+(1*3)=159
159 % 10 = 9
So 146399-33-9 is a valid CAS Registry Number.

146399-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methoxy-2-oxo-(3,5-di-tert-butyl)benzo-1,3,2-dioxaphospholin

1.2 Other means of identification

Product number -
Other names 4,6-Di-tert-butyl-2-methoxy-benzo[1,3,2]dioxaphosphole 2-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:146399-33-9 SDS

146399-33-9Relevant academic research and scientific papers

Semiquantitative Determination of Quinonoid Structures in Isolated Lignins by 31P Nuclear Magnetic Resonance

Argyropoulos, Dimitris S.,Zhang, Liming

, p. 4628 - 4634 (2007/10/03)

A semiquantitative analytical method has been developed for the determination of the total quinonoid content (o-benzoquinones and p-benzoquinones) of soluble lignins. The method is based on detailed measurements and observations made with model o- and p-quinones, which in dry organic solvents were shown to form adducts with trimethyl phosphite in quantitative yield. These adducts gave 31P NMR signals for o- and p-quinones at around -46 and -2 ppm, respectively. In the presence of moisture and lignin the adducts from o-quinones were shown to be hydrolyzed to the open ring product, dimethylphenyl phosphate (-2 ppm), at an overall yield of ~70%. Similarly, the hydrolysis yields of p-quinone adducts with trimethyl phosphite were ~70%. Consequently, a number of important issues in relation to the use of trimethyl phosphite toward the quantitative analysis of quinonoid groups in lignins have been investigated, which permitted the development of an experimental semiquantitative protocol recommended for spectral acquisition.

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