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1-isopropyl-3-(trifluoroMethyl)pyrazole-5-boronic acid is an organoboron compound characterized by a molecular formula of C9H12BF3N2O2. It features a pyrazole ring with a boronic acid functional group, which endows it with unique chemical properties and reactivity. 1-isopropyl-3-(trifluoroMethyl)pyrazole-5-boronic acid is widely recognized for its applications in organic synthesis and medicinal chemistry, where it serves as a versatile building block for the development of new pharmaceuticals and agrochemicals. Its potential in disease treatment and as a tool for biological research further underscores its significance in the scientific community.

1361380-69-9

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1361380-69-9 Usage

Uses

Used in Pharmaceutical and Agrochemical Development:
1-isopropyl-3-(trifluoroMethyl)pyrazole-5-boronic acid is utilized as a key building block in the synthesis of novel pharmaceuticals and agrochemicals. Its unique structure and reactivity allow for the creation of diverse molecules with potential therapeutic and pesticidal properties, contributing to the advancement of healthcare and agriculture.
Used in Organic Synthesis:
In the field of organic synthesis, 1-isopropyl-3-(trifluoroMethyl)pyrazole-5-boronic acid is employed as a valuable reagent. Its boronic acid moiety enables participation in Suzuki-Miyaura cross-coupling reactions, a widely used method for the formation of carbon-carbon bonds. This capability makes it an essential component in the synthesis of complex organic molecules and the development of new chemical entities.
Used in Disease Treatment Research:
1-isopropyl-3-(trifluoroMethyl)pyrazole-5-boronic acid has demonstrated potential applications in the treatment of various diseases. Its unique chemical properties allow for the design and synthesis of molecules with therapeutic potential, offering new avenues for the development of treatments for a range of medical conditions.
Used in Biological Research:
As a tool for studying biological processes, 1-isopropyl-3-(trifluoroMethyl)pyrazole-5-boronic acid aids in understanding the mechanisms of disease, the interactions between molecules, and the development of new diagnostic and therapeutic strategies. Its versatility and reactivity make it a valuable asset in the pursuit of scientific knowledge and the improvement of human health.

Check Digit Verification of cas no

The CAS Registry Mumber 1361380-69-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,3,8 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1361380-69:
(9*1)+(8*3)+(7*6)+(6*1)+(5*3)+(4*8)+(3*0)+(2*6)+(1*9)=149
149 % 10 = 9
So 1361380-69-9 is a valid CAS Registry Number.
InChI:InChI=1S/C7H10BF3N2O2/c1-4(2)13-6(8(14)15)3-5(12-13)7(9,10)11/h3-4,14-15H,1-2H3

1361380-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-Isopropyl-3-(trifluoromethyl)-1H-pyrazol-5-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

Emergency phone number -
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More Details:1361380-69-9 SDS

1361380-69-9Downstream Products

1361380-69-9Relevant academic research and scientific papers

ACYLAMINO BRIDGED HETEROCYCLIC COMPOUND, AND COMPOSITION AND APPLICATION THEREOF

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Paragraph 0105, (2021/11/04)

Provided are an acylamino bridged heterocyclic compound of formula (I) or a pharmaceutically acceptable salt, an isomer, a solvate, a crystal, or a prodrug thereof, and a pharmaceutical composition comprising the compound, and an application of the compou

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