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(4-[(Diethylamino)methyl]thiophen-2-yl)boronic acid is a chemical compound characterized by the molecular formula C12H17BNO2S. It features a boronic acid group, which is known for its ability to form covalent bonds with diols and amines, making it a versatile component in organic synthesis and pharmaceutical research. The presence of the thiophen-2-yl group in the molecule adds potential utility in the development of new materials or as a building block for more complex organic molecules. Furthermore, the diethylamino group contributes specific chemical properties to the compound, enhancing its suitability for a range of applications. Overall, (4-[(Diethylamino)methyl]thiophen-2-yl)boronic acid emerges as a promising compound with valuable applications in chemical and pharmaceutical research.

1142946-83-5

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1142946-83-5 Usage

Uses

Used in Organic Synthesis:
(4-[(Diethylamino)methyl]thiophen-2-yl)boronic acid is used as a synthetic building block for the creation of complex organic molecules. Its ability to form covalent bonds with diols and amines makes it a valuable component in the synthesis of various compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-[(Diethylamino)methyl]thiophen-2-yl)boronic acid is used as a key intermediate in the development of new drugs. Its unique chemical properties, including the boronic acid group and the diethylamino group, allow for the design and synthesis of novel therapeutic agents.
Used in Material Science:
The presence of the thiophen-2-yl group in (4-[(Diethylamino)methyl]thiophen-2-yl)boronic acid makes it potentially useful in the development of new materials. It can be employed as a building block for the creation of advanced materials with specific properties, such as conductivity or optical characteristics, depending on the desired application.
Used in Chemical Research:
(4-[(Diethylamino)methyl]thiophen-2-yl)boronic acid serves as a valuable tool in chemical research, where it can be utilized to study the properties and reactivity of boronic acid-containing compounds. This understanding can lead to the development of new synthetic methods and the discovery of novel chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1142946-83-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,2,9,4 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1142946-83:
(9*1)+(8*1)+(7*4)+(6*2)+(5*9)+(4*4)+(3*6)+(2*8)+(1*3)=155
155 % 10 = 5
So 1142946-83-5 is a valid CAS Registry Number.

1142946-83-5Upstream product

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