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73916-07-1

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73916-07-1 Usage

Description

(E)-2-(4-Methoxystyryl)-5-methyl benzoxazole, also known as 4-methoxystyryl-5-methyl-2-benzoxazole, is a chemical compound with a molecular formula of C17H15NO2. It is a fluorescent dye molecule that is commonly used in research and industrial applications as a fluorescent probe for detecting and imaging biological structures and processes. (E)-2-(4-Methoxystyryl)-5-methyl benzoxazole exhibits strong absorption and emission in the visible spectrum, making it an ideal candidate for fluorescence microscopy and other imaging techniques. It is also known for its high quantum yield and photostability, making it a reliable and versatile tool for fluorescence-based applications.

Uses

Used in Research and Industrial Applications:
(E)-2-(4-Methoxystyryl)-5-methyl benzoxazole is used as a fluorescent probe for detecting and imaging biological structures and processes. Its strong absorption and emission in the visible spectrum, along with its high quantum yield and photostability, make it a reliable and versatile tool for fluorescence microscopy and other imaging techniques.
Used in Photodynamic Therapy:
(E)-2-(4-Methoxystyryl)-5-methyl benzoxazole has been studied for its potential therapeutic applications, including its ability to act as a photosensitizer for photodynamic therapy in cancer treatment. This application takes advantage of the compound's strong absorption and emission properties, as well as its photostability, to target and destroy cancer cells with minimal damage to surrounding healthy tissue.
Used in Pharmaceutical Research:
(E)-2-(4-Methoxystyryl)-5-methyl benzoxazole's strong fluorescence properties and potential therapeutic applications make it a valuable tool in the development of new drugs and therapies. Researchers can use (E)-2-(4-Methoxystyryl)-5-methyl benzoxazole to study the interactions of various biological molecules and to develop new methods for drug delivery and targeting.
Used in Material Science:
(E)-2-(4-Methoxystyryl)-5-methyl benzoxazole's strong absorption and emission properties, as well as its photostability, make it a potential candidate for the development of new materials with unique optical properties. These materials could have applications in various industries, such as electronics, photonics, and sensing technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 73916-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,1 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73916-07:
(7*7)+(6*3)+(5*9)+(4*1)+(3*6)+(2*0)+(1*7)=141
141 % 10 = 1
So 73916-07-1 is a valid CAS Registry Number.

73916-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(E)-2-(4-methoxyphenyl)ethenyl]-5-methyl-1,3-benzoxazole

1.2 Other means of identification

Product number -
Other names -

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:73916-07-1 SDS

73916-07-1Downstream Products

73916-07-1Relevant articles and documents

2-STYRYLBENZOXAZOLE DERIVATIVES

Arient, Josef

, p. 3160 - 3165 (2007/10/02)

A series of 35 derivatives of 2-styrylbenzoxazole I-XXXV with methyl, chloro, hydroxy, methoxy, dimethylamino, nitro, cyano and methoxycarbonyl substituents have been prepared by reaction of substituted 2-acetamidophenol with respective benzaldehyde derivatives.

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