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6-cyanobenzo[b]thiophen-2-ylboronic acid is a boronic acid derivative with the molecular formula C9H6BClNO2S. It features a cyanobenzo[b]thiophene group, which contributes unique electronic and physicochemical properties to the molecule. Known for its reactivity in Suzuki-Miyaura cross-coupling reactions, 6-cyanobenzo[b]thiophen-2-ylboronic acid serves as a valuable building block in organic synthesis. Its potential applications extend to medicinal chemistry, where it has been investigated for enzyme inhibition and modulation of cell signaling pathways, as well as in materials science and electronic applications.

1119899-35-2

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1119899-35-2 Usage

Uses

Used in Organic Synthesis:
6-cyanobenzo[b]thiophen-2-ylboronic acid is used as a building block in organic synthesis for its reactivity in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds and the creation of a wide range of organic compounds.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 6-cyanobenzo[b]thiophen-2-ylboronic acid is used as a potential enzyme inhibitor and modulator of cell signaling pathways. Its unique structure allows it to interact with biological targets, offering opportunities for the development of new therapeutic agents.
Used in Materials Science:
6-cyanobenzo[b]thiophen-2-ylboronic acid is utilized in materials science for its specific electronic and physicochemical properties, which may contribute to the development of novel materials with tailored characteristics for various applications.
Used in Electronic Applications:
6-cyanobenzo[b]thiophen-2-ylboronic acid's electronic properties make it a candidate for use in electronic applications, where it could be integrated into devices or systems to enhance performance or enable new functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 1119899-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,9,8,9 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1119899-35:
(9*1)+(8*1)+(7*1)+(6*9)+(5*8)+(4*9)+(3*9)+(2*3)+(1*5)=192
192 % 10 = 2
So 1119899-35-2 is a valid CAS Registry Number.

1119899-35-2SDS

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 (6-Cyano-1-benzothiophen-2-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 6-cyano-benzothiophene-2-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:1119899-35-2 SDS

1119899-35-2Relevant academic research and scientific papers

THIAZOLIDINONE COMPOUNDS, AND METHODS OF MAKING AND USING SAME

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Page/Page column 43-44, (2009/04/25)

Provided herein are thiazolidinone compounds, and methods of making and using the same. Such compounds may be used in inflammatory or immune-mediated disorders. The disclosure provides for treating respiratory or ocular disorders, treating arthritis, or may be used to treat cancer, such as prostate or breast cancer, or multiple myeloma.

PYRROLOPYRIMIDINE COMPOUNDS AND THEIR USE AS JANUS KINASE MODULATORS

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Page/Page column 89, (2009/05/28)

Provided herein are pyrrolopyrimidine compounds of Formula (I) wherein R1 is a heteroaryl containing at least one S atom, and optionally substituted on a ring carbon by one, two, or three substituents each independently selected from the group consisting of : halo, hydroxyl, nitro, formyl, formamido, cyano, sulfonyl, carboxy, amino, amido, acylamino, carbamoyl, sulphamoyl, alkyl, alkenyl, CF3, ureido, alkynyl, alkoxy, alkanoyl, alkoxycarbonyl, carbaldehyde oxime, N -alkylsulphamoyl, N-alkylcarbamoyl, -OR13R11 or -R13R11; R2 is phenyl or pyridinyl, wherein R2 optionally substituted on a ring carbon by one, two, or three substituents each indenpendently selected from the group consisting of : halo, hydroxyl, cyano, nitro, formyl, formamido, carboxy, sulfonyl, amino, amido, -N- alkyl -amino, carbamoyl, sulphamoyl, CF3, ureido, alkyl, alkenyl, alkynyl, alkoxy, alkanoyl, alkoxycarbonyl, N-alkylsulphamoyl, N-alkylcarbamoyl, -OR11, -OR12R11, or -R12R11; and methods of making and using the same. Such compounds may be used in inflammatory or myeloproliferative disorders. The disclosure also provides for treating cancer.

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