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Dibenzofuran-4,6-diborate is an organoboron compound featuring a dibenzofuran core, which is a system of fused aromatic rings, with boron elements attached at the 4,6-positions. It is known for its versatility in synthetic chemistry and can be used as a reagent in various chemical reactions, particularly for the synthesis of complex organic molecules.

145238-17-1

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145238-17-1 Usage

Uses

Used in Organic Chemistry:
Dibenzofuran-4,6-diborate is used as a reagent for the synthesis of complex organic molecules, leveraging its unique structure and properties to facilitate various chemical reactions.
Used in Pharmaceutical Industry:
Although the specific applications are not detailed, the potential of Dibenzofuran-4,6-diborate in the pharmaceutical industry could be related to its use in the development of new drugs or drug delivery systems, given the importance of organoboron compounds in medicinal chemistry.
Used in Material Science:
The versatility of Dibenzofuran-4,6-diborate may extend to material science, where it could be employed in the creation of novel materials with specific properties, such as improved conductivity or stability, by incorporating its structure into the material's composition.

Check Digit Verification of cas no

The CAS Registry Mumber 145238-17-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,3 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 145238-17:
(8*1)+(7*4)+(6*5)+(5*2)+(4*3)+(3*8)+(2*1)+(1*7)=121
121 % 10 = 1
So 145238-17-1 is a valid CAS Registry Number.

145238-17-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dibenzofuran-4,6-bis-(boronic acid)

1.2 Other means of identification

Product number -
Other names Dibenzofuran-4,6-diborate

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:145238-17-1 SDS

145238-17-1Relevant academic research and scientific papers

New organic electroluminescent compound and organic electroluminescent device comprising the same

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Paragraph 0130-0131, (2020/12/23)

The present invention relates to a novel organic electroluminescent compound and an organic light emitting device comprising the same. When the compound according to the present invention is used as a host material in a phosphorescent light emitting layer

New organic electroluminescent compound and organic electroluminescent device comprising the same

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Paragraph 0107-0110, (2020/12/25)

The present invention relates to a novel organic electroluminescent compound and an organic light emitting device comprising the same. When the compound according to the present invention is used as a host material in a phosphorescent light emitting layer

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENTS, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE

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Paragraph 0358; 0359, (2016/06/06)

A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different.

LADDER COMPOUND, AND ORGANIC ELECTROLUMINESCENT ELEMENT USING SAME

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Paragraph 0222-0225, (2016/11/02)

A compound represented by the following formula (1). In the formula (1), when Ar1 and Ar2 are the same substituents, as for all of the following pairs: Y1 and Y12, Y2 and Y11, Y3 and Y10, Y4 and Y9, Y5 and Y8, and Y6 and Y7, Y1 to Y12 of each pair are not the same as each other.

AMINE COMPOUND HAVING HETERO-FUSED RING AND ORGANIC ELECTROLUMINESCENT ELEMENT USING AMINE COMPOUND

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Paragraph 0183-0186, (2016/10/09)

A compound represented by the following formula (1).

Synthesis of [2]catenanes by oxidative intramolecular diyne coupling mediated by macrocyclic copper(I) complexes

Sato, Yuta,Yamasaki, Ryu,Saito, Shinichi

supporting information; experimental part, p. 504 - 507 (2009/04/14)

(Chemical Equation Presented) Right said thread: Oxidative intramolecular coupling reactions of α,ω-diynes in the presence of macrocyclic phenanthroline CuI complexes allows the synthesis of [2]catenanes in up to 64% yield (see scheme). The bon

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