1007375-81-6

Basic information

• Product Name: 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]thiazole
• Synonyms: 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]thiazole
• CAS NO: 1007375-81-6
• Molecular Weight: 337.25
• Mol File: 1007375-81-6.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]thiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]thiazole(1007375-81-6)
• EPA Substance Registry System: 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]thiazole(1007375-81-6)

Safety Data

• Hazardous Substances Data: 1007375-81-6(Hazardous Substances Data)

Usage

General Description

2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]thiazole, also known as BODIPY (4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene), is a fluorescent dye that is commonly used in biological imaging and sensing applications. The compound contains a boron-dipyrromethene core, which gives it its fluorescent properties. BODIPY dyes have a high quantum yield and are known for their photostability, making them ideal for long-term imaging experiments. Additionally, their spectral properties can be easily modified by changing the substituents on the phenyl rings, allowing for customization of the dye for specific applications. Overall, BODIPY dyes are versatile and widely used in a variety of scientific research and medical applications.

Upstream product

• 615-20-3 2-chlorobenzo[d][1,3]thiazole 
• 6265-91-4 2-(4-chlorophenyl)benzothiazole 
• 73183-34-3 bis(pinacol)diborane 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 19654-19-4 2-(4-bromophenyl)benzothiazole 
• 586-75-4 4-chlorobenzoyl chloride 
• 137-07-5 2-amino-benzenethiol 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 1259883-27-6 C₃₉H₃₀N₂S 
• 1268613-32-6 C₄₆H₂₈N₄S₂ 

Relevant articles and documents

Improving organic memory performance through mounting conjugated branches on a triphenylamine core

To study the influence of the number of branches mounted on molecular backbones on the thin-film morphology and performance of their memory devices, we successfully synthesized three conjugated small molecules containing triphenylamine and benzothiazole m

Star-shaped glycosylated conjugated oligomer for two-photon fluorescence imaging of live cells

A star-shaped glycosylated conjugated oligomer, 4,4′,4″-tris(4- (2-(4-(benzo[d]thiazol-2-yl)phenyl)-9,9′-bis(6-thiol-β-d-glucose) -hexyl)-fluoren-7-yl)phenylamine (TFBS), is synthesized for two-photon fluorescence imaging of live cells. The high density o

Benzazole derivatives and organic electroluminescent device including the same

Provided is a benzazole derivative which effectively absorbs a high-energy external light source in the UV region and thus minimizes damage to organic materials in an organic electroluminescent device, thereby contributing to a substantial improvement in the service life of the organic electroluminescent device. An organic electroluminescent device according to the present invention comprises: a first electrode; a second electrode; at least one organic layer disposed between the first electrode and the second electrode; and a capping layer, wherein the organic layer or the capping layer comprises a benzazole derivative represented by chemical formula 1 according to the present invention.

Structure-property relationship in multi-stimuli responsive D-A-A′ benzothiazole functionalized isomers

Multichromophoric D-A-A′ molecules comprising of benzothiazole (BT) as A′, benzothiadiazole (BTD) as A and tetraphenylethylene (TPE) as D were designed and synthesized as positional isomers p-BT, m-BT and o-BT by attaching the BTD-TPE moiety ortho, meta a