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Tris(4-methoxy-3,5-dimethyl phenyl)boroxine is a complex organic compound with the chemical formula C27H33BO3. It is a derivative of boroxine, which is a type of boron-containing compound. This specific boroxine features three 4-methoxy-3,5-dimethyl phenyl groups attached to a central boron atom. The compound is characterized by its aromatic structure, with each phenyl group containing a methoxy group at the 4-position and two methyl groups at the 3 and 5 positions. Tris(4-methoxy-3,5-dimethyl phenyl)boroxine is known for its potential applications in materials science, particularly in the development of polymers and as a ligand in coordination chemistry. Its unique structure contributes to its stability and reactivity, making it a subject of interest for researchers in the field of organic and inorganic chemistry.

34907-43-2

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34907-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34907-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,0 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34907-43:
(7*3)+(6*4)+(5*9)+(4*0)+(3*7)+(2*4)+(1*3)=122
122 % 10 = 2
So 34907-43-2 is a valid CAS Registry Number.

34907-43-2SDS

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 tris(4-methoxy-3.5-dimethyl phenyl)boroxine

1.2 Other means of identification

Product number -
Other names Tris(4-methoxy-3.5-dimethylphenyl)boroxin

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

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More Details:34907-43-2 SDS

34907-43-2Relevant academic research and scientific papers

Formation of hetero-boroxines: Dynamic combinatorial libraries generated through trimerization of pairs of arylboronic acids

Tokunaga, Yuji,Ueno, Hiroki,Shimomura, Youji

, p. 219 - 223 (2008/09/17)

Condensation of pairs of arylboronic acids provided homo- and hetero-boroxines in solution as evidenced from NMR spectra, and those boroxines were detected in the gas phase by GC-MS spectrometry. Equilibrium constants for the formation of these boroxines in solution were obtained through integration of pertinent signals in the NMR spectra of the mixtures ofboronic acids.

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