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5-Trifluoromethyl-thiophene-2-boronic acid is a chemical compound with the molecular formula C6H4BF3O2S. It is a boronic acid derivative that contains a thiophene ring and a trifluoromethyl group. 5-Trifluoromethyl-thiophene-2-boronic acid is known for its unique properties and versatility in chemical reactions due to the presence of the boronic acid functional group and the trifluoromethyl group.

958451-91-7

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958451-91-7 Usage

Uses

Used in Organic Synthesis:
5-Trifluoromethyl-thiophene-2-boronic acid is used as a building block in organic synthesis for creating more complex molecules. Its ability to form stable complexes with other molecules makes it a valuable component in constructing intricate chemical structures.
Used in Pharmaceutical Research and Drug Discovery:
In the pharmaceutical industry, 5-Trifluoromethyl-thiophene-2-boronic acid is used as a key intermediate in the development of new therapeutic agents. Its unique properties and reactivity contribute to the design and synthesis of potential drugs with novel mechanisms of action.
Used in Chemical Reactions:
The boronic acid functional group in 5-Trifluoromethyl-thiophene-2-boronic acid allows it to participate in various chemical reactions, such as Suzuki-Miyaura cross-coupling, which is widely used for the formation of carbon-carbon bonds. This makes the compound an important tool in the synthesis of a wide range of organic compounds.
Used in Medicinal Chemistry:
The presence of the trifluoromethyl group in 5-Trifluoromethyl-thiophene-2-boronic acid can impart unique properties to the compound, making it valuable for applications in medicinal chemistry. This group can influence the lipophilicity, metabolic stability, and binding affinity of the resulting molecules, which is crucial for the development of effective drugs.
Overall, 5-Trifluoromethyl-thiophene-2-boronic acid is a versatile and valuable compound in the fields of organic synthesis, pharmaceutical research, and medicinal chemistry, owing to its unique structural features and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 958451-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,4,5 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 958451-91:
(8*9)+(7*5)+(6*8)+(5*4)+(4*5)+(3*1)+(2*9)+(1*1)=217
217 % 10 = 7
So 958451-91-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H4BF3O2S/c7-5(8,9)3-1-2-4(12-3)6(10)11/h1-2,10-11H

958451-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(trifluoromethyl)thiophen-2-yl]boronic acid

1.2 Other means of identification

Product number -
Other names 5-Trifluoromethyl-thiophene-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:958451-91-7 SDS

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