structure of Thiazol-2-ylboronic acid

Thiazol-2-ylboronic acid

CAS No.: 389630-95-9
M. Wt: 128.945
M. Fa: C3H4BNO2S
InChI Key: JWUGKJKBCKJFOU-UHFFFAOYSA-N

Names and Identifiers of Thiazol-2-ylboronic acid

CAS Number

389630-95-9

IUPAC Name

1,3-thiazol-2-ylboronic acid

InChI

InChI=1S/C3H4BNO2S/c6-4(7)3-5-1-2-8-3/h1-2,6-7H

InChIKey

JWUGKJKBCKJFOU-UHFFFAOYSA-N

Canonical SMILES

B(C1=NC=CS1)(O)O

Physical and chemical properties of Thiazol-2-ylboronic acid

Acidity coefficient

7.68±0.53(Predicted)

Boiling Point

320.9±25.0 °C at 760 mmHg

Density

1.4±0.1 g/cm3

Exact Mass

129.005585

Flash Point

147.9±23.2 °C

Index of Refraction

1.565

LogP

0.76

Molecular Formula

C3H4BNO2S

Molecular Weight

128.945

PSA

81.59000

Vapour Pressure

0.0±0.7 mmHg at 25°C

Safety Information of Thiazol-2-ylboronic acid

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of Thiazol-2-ylboronic acid

Thiazol-2-ylboronic acid has several applications across different fields:

  • Organic Synthesis: It serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals through carbon-carbon bond formation.
  • Material Science: The compound is utilized in developing functional materials due to its ability to form stable complexes with various substrates.
  • Biological Research: Its derivatives are explored for their potential therapeutic effects against various diseases, including cancer and neurodegenerative disorders.

Interaction Studies of Thiazol-2-ylboronic acid

Studies focusing on the interactions of thiazol-2-ylboronic acid with biological targets have revealed its potential as an enzyme inhibitor. For instance, research has indicated that certain derivatives can effectively inhibit specific kinases involved in cell signaling pathways, which is crucial for developing new cancer therapies. Additionally, its interactions with proteins and nucleic acids are being investigated to understand its role in cellular processes better.

Biological Activity of Thiazol-2-ylboronic acid

Thiazol-2-ylboronic acid exhibits significant biological activity, particularly in medicinal chemistry. Compounds containing thiazole moieties are often investigated for their potential as antimicrobial agents, anti-inflammatory drugs, and inhibitors of various enzymes. For instance, derivatives of thiazole have been shown to inhibit certain kinases involved in cancer progression and are being explored for their therapeutic potential against diseases like Alzheimer's.