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1256345-99-9

2-Isobutoxy-5-(trifluoromethyl)phenylboronic acid is an organoboron compound, specifically a boronic acid, that is widely utilized in synthetic chemistry. This chemical is known for its reactivity in cross-coupling reactions, particularly Suzuki-Miyaura couplings, which are instrumental in the formation of carbon-carbon bonds. The presence of isobutoxy and trifluoromethyl groups on the phenyl ring significantly influences the chemical's reactivity and the properties of the compounds derived from it. With a molecular weight of 283.09 g/mol, 2-Isobutoxy-5-(trifluoromethyl)phenylboronic acid is typically found in crystalline powder form and should be handled with caution due to its potential hazards.

1256345-99-9

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1256345-99-9 Usage

Uses

Used in Synthetic Chemistry:
2-Isobutoxy-5-(trifluoromethyl)phenylboronic acid is used as a key component in various chemical reactions, particularly in the field of synthetic chemistry. Its boronic acid functional group provides valuable reactivity, making it a versatile tool for the synthesis of complex organic molecules.
Used in Cross-Coupling Reactions:
In the realm of cross-coupling reactions, 2-Isobutoxy-5-(trifluoromethyl)phenylboronic acid is used as a reagent for the formation of carbon-carbon bonds. Its participation in Suzuki-Miyaura couplings is particularly noteworthy, as these reactions are widely employed in the synthesis of biologically active compounds and pharmaceuticals.
Used in Pharmaceutical Synthesis:
2-Isobutoxy-5-(trifluoromethyl)phenylboronic acid is used as an intermediate in the synthesis of pharmaceutical compounds. The unique combination of isobutoxy and trifluoromethyl groups on the phenyl ring allows for the creation of molecules with specific properties, which can be crucial for the development of new drugs and therapeutic agents.
Used in Material Science:
In the field of material science, 2-Isobutoxy-5-(trifluoromethyl)phenylboronic acid is used as a building block for the development of new materials with tailored properties. The reactivity of the boronic acid group and the presence of the isobutoxy and trifluoromethyl groups enable the creation of materials with unique characteristics, such as improved stability or enhanced electronic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1256345-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,4 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1256345-99:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*4)+(3*5)+(2*9)+(1*9)=169
169 % 10 = 9
So 1256345-99-9 is a valid CAS Registry Number.

1256345-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Isobutoxy-5-(trifluoromethyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names [2-(2-methylpropoxy)-5-(trifluoromethyl)phenyl]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:1256345-99-9 SDS

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