CAS 1310384-98-5

2-(3-Methoxy-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:

2-(3-Methoxy-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structure, which includes a dioxaborolane ring and a thienyl group. This compound features a boron atom coordinated to two oxygen atoms within a five-membered ring, contributing to its stability and reactivity. The presence of the methoxy group enhances its solubility in organic solvents and may influence its electronic properties, making it potentially useful in various applications, including organic synthesis and materials science. The thienyl moiety can impart interesting electronic characteristics, making this compound a candidate for use in organic electronics or as a building block in the synthesis of more complex molecules. Additionally, the tetramethyl substitution on the dioxaborolane ring can affect its steric and electronic properties, influencing its reactivity and interactions with other chemical species. Overall, this compound exemplifies the diverse chemistry of boron compounds and their potential utility in advanced materials and organic synthesis.

Formula: C₁₁H₁₇BO₃S

InChI: InChI=1S/C11H17BO3S/c1-10(2)11(3,4)15-12(14-10)9-8(13-5)6-7-16-9/h6-7H,1-5H3

InChI key: InChIKey=FXKKXDGOIQJEJS-UHFFFAOYSA-N

SMILES: O(C)C1=C(SC=C1)B2OC(C)(C)C(C)(C)O2

Synonyms:

• 2-(3-Methoxy-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• 3-Methoxythiophene-2-boronic acid pinacol ester
• 3-Methoxythiophen-2-ylboronic acid pinacol ester
• 1,3,2-Dioxaborolane, 2-(3-methoxy-2-thienyl)-4,4,5,5-tetramethyl-

3-Methoxythiophene-2-boronic acid pinacol ester

CAS: 1310384-98-5

Formula: C₁₁H₁₇BO₃S

Purity: 97%

Color and Shape: Solid

Molecular weight: 240.1269

Ref: IN-DA009BJ7

2-(3-Methoxythiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 1310384-98-5

2-(3-Methoxythiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Purity: 98%

Molecular weight: 240.13g/mol

Ref: 54-OR91442

3-Methoxythiophene-2-boronic acid pinacol ester

CAS: 1310384-98-5

3-Methoxythiophene-2-boronic acid pinacol ester is a ligand that can be used in the synthesis of organic molecules. It undergoes nucleophilic substitution reactions and has been shown to be an excellent substrate for Suzuki coupling reactions. This reactant can also be used as a backbone in the synthesis of optical materials, such as semiconductors. 3-Methoxythiophene-2-boronic acid pinacol ester is capable of forming a variety of substitutions and transfers with benzothiadiazole derivatives, which have been shown to have an acceptor effect on organic molecules.

Formula: C₁₁H₁₇BO₃S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 240.13 g/mol

Ref: 3D-KCC38498

2-(3-Methoxythiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 1310384-98-5

Purity: 97%

Color and Shape: Solid

Molecular weight: 240.1199951

Ref: 10-F696220