1310404-96-6

Basic information

• Product Name: 2-methylthiazol-4-ylboronic acid pinacol ester
• Synonyms: 2-methylthiazol-4-ylboronic acid pinacol ester;2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole;Thiazole, 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
• CAS NO: 1310404-96-6
• Molecular Formula: C₁₀H₁₆BNO₂S
• Molecular Weight: 243.13082
• Mol File: 1310404-96-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 312.1±15.0 °C(Predicted)
• Appearance: /
• Density: 1.10±0.1 g/cm3(Predicted)
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• PKA: 3.51±0.10(Predicted)
• CAS DataBase Reference: 2-methylthiazol-4-ylboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylthiazol-4-ylboronic acid pinacol ester(1310404-96-6)
• EPA Substance Registry System: 2-methylthiazol-4-ylboronic acid pinacol ester(1310404-96-6)

Safety Data

• Hazardous Substances Data: 1310404-96-6(Hazardous Substances Data)

Usage

General Description

2-Methylthiazol-4-ylboronic acid pinacol ester is a chemical compound used in organic synthesis and medicinal chemistry. It is a boronic acid derivative that contains a thiazole ring and a pinacol ester functional group. Boronic acids are valuable reagents in Suzuki-Miyaura cross-coupling reactions, which are widely used in the synthesis of pharmaceuticals and agrochemicals. The pinacol ester moiety provides stability to the boronic acid, making it a versatile building block for the synthesis of complex organic molecules. 2-Methylthiazol-4-ylboronic acid pinacol ester has been utilized in the development of various bioactive compounds and as an intermediate in the preparation of pharmaceutical drugs.

Downstream Products

• 1083245-91-3 2-(2-methylthiazol-4-yl)benzaldehyde