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5-Iodo-2-trifluoromethoxyphenylboronic acid is a chemical compound that features a boronic acid group attached to a phenyl ring, which is substituted with an iodine atom and a trifluoromethoxy group. 5-Iodo-2-trifluoromethoxyphenylboronic acid is recognized for its unique structure and reactivity, making it a versatile building block in organic synthesis and medicinal chemistry for the creation of diverse biologically active molecules.

1256355-12-0

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1256355-12-0 Usage

Uses

Used in Organic Synthesis:
5-Iodo-2-trifluoromethoxyphenylboronic acid is utilized as a building block in organic synthesis for the preparation of a broad spectrum of biologically active compounds. Its presence in the synthesis process allows for the creation of complex organic molecules with potential applications in various fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-Iodo-2-trifluoromethoxyphenylboronic acid is employed as a key intermediate for the development of pharmaceuticals. Its unique properties facilitate the synthesis of new drug candidates with improved therapeutic profiles.
Used in Palladium-Catalyzed Cross-Coupling Reactions:
5-Iodo-2-trifluoromethoxyphenylboronic acid is used as a powerful cross-coupling reagent in palladium-catalyzed reactions. This application is crucial for the formation of carbon-carbon and carbon-heteroatom bonds, which are fundamental in constructing the molecular frameworks of various chemical entities, including pharmaceuticals and agrochemicals.
Used in the Development of Fluorescent Probes and Sensors:
The boronic acid functionality of 5-Iodo-2-trifluoromethoxyphenylboronic acid makes it a valuable component in the development of fluorescent probes and sensors for biological applications. These tools are essential for studying biological processes and detecting specific biomolecules within complex biological systems.
Used in Specialty Chemicals Industry:
5-Iodo-2-trifluoromethoxyphenylboronic acid is also used in the specialty chemicals industry, where its unique structure and reactivity contribute to the synthesis of high-value chemical products with specific applications in various sectors, such as materials science, environmental science, and more.

Check Digit Verification of cas no

The CAS Registry Mumber 1256355-12-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1256355-12:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*5)+(2*1)+(1*2)=150
150 % 10 = 0
So 1256355-12-0 is a valid CAS Registry Number.

1256355-12-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-Iodo-2-(trifluoromethoxy)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 5-IODO-2-TRIFLUOROMETHOXYPHENYLBORONIC 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:1256355-12-0 SDS

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