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Boronic acid, B-[1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrrolo[2,3-b]pyridin-2-yl]-, is a complex chemical compound that features a boronic acid functional group attached to a pyrrolopyridine ring system. This unique structure is tailored for applications in organic synthesis and medicinal chemistry, where boronic acids serve as multifaceted building blocks for crafting intricate molecular structures. The incorporation of a trimethylsilyl group into the molecule enhances its reactivity and stability, positioning it as a potentially valuable asset in the development of innovative pharmaceuticals, agrochemicals, and advanced materials. The exploration of boronic acid derivatives like this one extends to their utility as enzyme inhibitors, fluorescent markers, and molecular sensors, highlighting their broad relevance in drug discovery and diagnostic applications.

1286776-82-6

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1286776-82-6 Usage

Uses

Used in Pharmaceutical Development:
Boronic acid, B-[1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrrolo[2,3-b]pyridin-2-yl]-, is utilized as a key intermediate in the synthesis of pharmaceuticals due to its ability to form stable complexes with biological targets, thereby enhancing the efficacy and selectivity of drug molecules.
Used in Agrochemical Synthesis:
In the agrochemical industry, this boronic acid derivative is employed as a building block for the creation of novel agrochemicals, leveraging its reactivity to improve the performance and selectivity of pesticides and other crop protection agents.
Used in Material Science:
Boronic acid, B-[1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrrolo[2,3-b]pyridin-2-yl]-, serves as a component in the development of new materials, where its unique properties can contribute to the creation of materials with enhanced properties such as sensitivity to environmental stimuli or improved mechanical characteristics.
Used as Enzyme Inhibitors:
Boronic acid, B-[1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrrolo[2,3-b]pyridin-2-yl]is explored for its potential as an enzyme inhibitor, where it can modulate the activity of specific enzymes involved in various biological processes, offering therapeutic benefits in treating enzyme-related diseases.
Used as Fluorescent Markers:
In the field of bioimaging and diagnostics, the boronic acid derivative is considered for use as a fluorescent marker, capitalizing on its optical properties to visualize and track biological processes at the molecular level.
Used as Molecular Sensors:
Boronic acid, B-[1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrrolo[2,3-b]pyridin-2-yl]is also examined for its application as a molecular sensor, detecting and responding to specific molecules or environmental changes, which can be instrumental in the development of responsive materials and diagnostic tools.

Check Digit Verification of cas no

The CAS Registry Mumber 1286776-82-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,6,7,7 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1286776-82:
(9*1)+(8*2)+(7*8)+(6*6)+(5*7)+(4*7)+(3*6)+(2*8)+(1*2)=216
216 % 10 = 6
So 1286776-82-6 is a valid CAS Registry Number.

1286776-82-6SDS

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 [1-(2-trimethylsilylethoxymethyl)pyrrolo[2,3-b]pyridin-2-yl]boronic acid

1.2 Other means of identification

Product number -
Other names -

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:1286776-82-6 SDS

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