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2-phenyl-1,3,2-dioxaborepane is an organic compound characterized by a unique structure that includes a boron atom, two oxygen atoms, and a phenyl group. This molecule is a heterocyclic compound, specifically a dioxaborepane, which means it contains a boron atom bonded to two oxygen atoms, forming a three-membered ring. The phenyl group is attached to the boron, contributing to the compound's aromatic properties. Such compounds are of interest in organic chemistry and materials science due to their potential applications in the synthesis of various chemical products and as intermediates in complex organic reactions. The specific properties and reactivity of 2-phenyl-1,3,2-dioxaborepane can be influenced by the electronic and steric effects of the phenyl group, making it a subject of study for its potential use in the development of new materials or pharmaceuticals.

4406-76-2

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4406-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4406-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4406-76:
(6*4)+(5*4)+(4*0)+(3*6)+(2*7)+(1*6)=82
82 % 10 = 2
So 4406-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BO2/c1-2-6-10(7-3-1)11-12-8-4-5-9-13-11/h1-3,6-7H,4-5,8-9H2

4406-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1,3,2-dioxaborepane

1.2 Other means of identification

Product number -
Other names 1,3,2-Dioxaborepane,2-phenyl

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:4406-76-2 SDS

4406-76-2Downstream Products

4406-76-2Relevant academic research and scientific papers

Diol lipids - Communication 27. Identification of C2-C4-diols in the form of cyclic esters of phenylboric acid by the method of combined gas chromatography and mass spectrometry

Batrakov,Panosyan,Ushakov,Rozynov,Bergel'son

, p. 1662 - 1668 (2007/10/10)

1. A new method was proposed for the analysis of small quantities of C2-C4-diols, formed in the cleavage of lipids, based on combined gas-chromatography and mass spectrography of their phenylborate esters. 2. Phenylborate esters of d

The structure of the benzeneboronate of pentane-1,3,5-triol

Bourne, Edward J.,Mckinley, Ian R.,Weigel, Helmut

, p. 141 - 149 (2007/10/16)

The relative ease of formation of five-, six-, seven-, and eight-membered cyclic benzeneboronates is discussed. Pentane-1,3,5-triol forms, by interaction with benzene-boronic anhydride, exclusively DL-4-(2-hydroxyethyl)-2-phenyl-1,3,2-dioxaborinane. It is suggested that, in this compound, the oxygen atom of the hydroxyl group is intramolecularly co-ordinated with the boron atom.

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