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1,3-DIOXA-2-(2-BROMOMETHYLPHENYL)-BORINANE is a chemical compound characterized by the presence of a boron atom and a dioxane ring structure. It is recognized for its role as a Lewis acid catalyst in organic synthesis, with the bromomethylphenyl group endowing it with unique reactivity suitable for nucleophilic substitution and cross-coupling reactions. 1,3-DIOXA-2-(2-BROMOMETHYLPHENYL)-BORINANE holds promise for applications across various industries, including pharmaceuticals and materials science, while requiring careful handling due to its reactive nature and potential hazards.

174900-86-8

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174900-86-8 Usage

Uses

Used in Organic Synthesis:
1,3-DIOXA-2-(2-BROMOMETHYLPHENYL)-BORINANE is used as a reagent for its Lewis acid catalytic properties, facilitating various organic reactions that require the activation of certain functional groups or the promotion of specific reaction pathways.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,3-DIOXA-2-(2-BROMOMETHYLPHENYL)-BORINANE is utilized as a key intermediate in the synthesis of complex organic molecules, including potential drug candidates, due to its ability to participate in cross-coupling and nucleophilic substitution reactions.
Used in Agrochemical Industry:
Similarly, in agrochemicals, 1,3-DIOXA-2-(2-BROMOMETHYLPHENYL)-BORINANE serves as a precursor in the development of new pesticides or other agrochemical products, leveraging its reactivity to form novel and effective compounds.
Used in Advanced Materials Production:
1,3-DIOXA-2-(2-BROMOMETHYLPHENYL)-BORINANE is also used as a component in the creation of advanced materials, where its unique structure and reactivity contribute to the development of materials with specific properties for high-tech applications.
It is crucial for chemists and researchers to handle 1,3-DIOXA-2-(2-BROMOMETHYLPHENYL)-BORINANE with appropriate safety measures, given its reactivity and potential risks associated with its use in chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 174900-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,9,0 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 174900-86:
(8*1)+(7*7)+(6*4)+(5*9)+(4*0)+(3*0)+(2*8)+(1*6)=148
148 % 10 = 8
So 174900-86-8 is a valid CAS Registry Number.

174900-86-8SDS

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 2-[2-(bromomethyl)phenyl]-1,3,2-dioxaborinane

1.2 Other means of identification

Product number -
Other names OR7213

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:174900-86-8 SDS

174900-86-8Downstream Products

174900-86-8Relevant academic research and scientific papers

Boronic acid based photoinduced electron transfer (PET) fluorescence sensors for saccharides

Larkin, Joseph D.,Frimat, Karine A.,Fyles, Thomas M.,Flower, Stephen E.,James, Tony D.

, p. 2922 - 2931 (2010)

A simple three step synthesis was developed to provide six novel modular sensors, consisting of three para sensors, and three meta sensors with naphthalene, anthracene and pyrene fluorophores. The interaction of the six sensors with the saccharides: d-glu

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