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Boronic acid, [4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl](9CI) is a complex chemical compound that features a boronic acid group and a 4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl group. Boronic acid, [4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl](9CI) is recognized for its versatile applications in organic synthesis and medicinal chemistry, where it serves as a fundamental building block for the creation of a wide array of pharmaceuticals and agrochemicals. Its potential in developing new treatments for various diseases, including cancer and infectious diseases, is noteworthy. Furthermore, it shows promise in the realm of material science and sensor technology due to its unique properties.

685513-99-9

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685513-99-9 Usage

Uses

Used in Pharmaceutical Industry:
Boronic acid, [4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl](9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of diverse drug molecules. Its unique structure allows for the development of new treatments targeting a range of diseases, particularly cancer and infectious diseases, by enhancing the efficacy and selectivity of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, Boronic acid, [4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl](9CI) is utilized as a building block in the synthesis of agrochemicals, contributing to the development of novel compounds for pest control and crop protection. Its role in this industry is crucial for enhancing the effectiveness of agrochemicals and ensuring sustainable agricultural practices.
Used in Material Science:
Boronic acid, [4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl](9CI) is employed in material science for the development of new materials. Its unique chemical properties make it suitable for creating advanced materials with specific characteristics required for various applications, such as high-performance polymers and composites.
Used in Sensor Technology:
In the field of sensor technology, Boronic acid, [4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl](9CI) is used for the development of new sensors. Its chemical reactivity and selectivity make it an ideal candidate for the design of sensors that can detect and measure various analytes with high sensitivity and specificity, contributing to advancements in environmental monitoring, medical diagnostics, and industrial process control.

Check Digit Verification of cas no

The CAS Registry Mumber 685513-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,5,1 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 685513-99:
(8*6)+(7*8)+(6*5)+(5*5)+(4*1)+(3*3)+(2*9)+(1*9)=199
199 % 10 = 9
So 685513-99-9 is a valid CAS Registry Number.

685513-99-9SDS

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 Boronic acid, [4-chloro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridin-5-yl]- (9CI)

1.2 Other means of identification

Product number -
Other names (4-Chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)boronic acid

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:685513-99-9 SDS

685513-99-9Downstream Products

685513-99-9Relevant academic research and scientific papers

Synthesis of functionalized 7-azaindoles via directed ortho-metalations

L'Heureux, Alexandre,Thibault, Carl,Ruel, Réjean

, p. 2317 - 2319 (2007/10/03)

Functionalization at C-5 of 4-fluoro- and 4-chloro-1-triisopropylsilyl-7- azaindole, 1 and 2, respectively, leads to a variety of new substituted 7-azaindole derivatives. We also describe two approaches to introduce functionality at C-6.

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