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(E)-2-Styrylbenzoxazole is a benzoxazole derivative that features a benzene ring connected to a benzoxazole ring through a styryl linker. This chemical compound is renowned for its bright blue fluorescence when exposed to ultraviolet light, which is attributed to its unique optical and electronic properties. Its ability to serve as a fluorescent probe in biological research and its potential in the development of materials for organic light-emitting diodes (OLEDs) and optoelectronic devices make it a significant compound in the field of organic synthesis and photonic applications.

78685-70-8

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78685-70-8 Usage

Uses

Used in Organic Synthesis:
(E)-2-Styrylbenzoxazole is used as a key intermediate in the synthesis of various organic compounds due to its unique structure and reactivity.
Used in Biological Research as a Fluorescent Probe:
(E)-2-Styrylbenzoxazole is utilized as a fluorescent label in biological research for its ability to emit bright blue fluorescence under ultraviolet light, aiding in the visualization and tracking of biological processes.
Used in the Development of Organic Light-Emitting Diodes (OLEDs):
(E)-2-Styrylbenzoxazole is employed in the development of materials for OLEDs, capitalizing on its optical and electronic properties to enhance the performance and efficiency of these devices.
Used in Optoelectronic Devices:
(E)-2-Styrylbenzoxazole is used in the creation of optoelectronic devices, leveraging its photophysical properties to improve the functionality and performance of such devices.
Used in Photonic Applications:
(E)-2-Styrylbenzoxazole's interesting photophysical properties make it a promising candidate for further studies and applications in the field of photonics, where its fluorescence and other characteristics can be harnessed for various technological advancements.

Check Digit Verification of cas no

The CAS Registry Mumber 78685-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,8 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78685-70:
(7*7)+(6*8)+(5*6)+(4*8)+(3*5)+(2*7)+(1*0)=188
188 % 10 = 8
So 78685-70-8 is a valid CAS Registry Number.

78685-70-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-Styrylbenzoxazole

1.2 Other means of identification

Product number -
Other names 2-styryl-benzooxazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78685-70-8 SDS

78685-70-8Downstream Products

78685-70-8Relevant academic research and scientific papers

Photochemical and Thermal Reactions of Aromatic Schiff Bases

Tauer, Erich,Grellmann, Karl H.

, p. 4252 - 4258 (2007/10/02)

The photochemical and thermal reactions of aromatic Schiff bases (SB) prepared from o-aminophenol and aldehydes and from o-aminophenol and ketones are compared.All SB's are converted by light into the corresponding benzoxazolines.For the SB's derived from aldehydes, benzoxazoline formation is a prerequisite to convert them by a second photon into benzoxazoles.In some cases oxygen is not required for this second reaction step.SB's derived from ketones are converted into benzoxazoles by the absorption of just one photon, but only in the presence of oxygen and only if the aliphatic residue R1 of the N=C(R1R2) bridge contains at least two carbon atoms.A radical mechanism is proposed for this reaction.Benzoxazine formation is observed in some cases as a thermal side reaction.The photochemical reactions of the latter were also investigated.

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