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Benzoxazole, 2-[2-(4-fluorophenyl)ethenyl]-, is a chemical compound with the molecular formula C15H10FNO and a molecular weight of 235.24 g/mol. It is a derivative of benzoxazole, which is a heterocyclic aromatic compound consisting of a benzene ring fused to an oxazole ring. The compound features a 4-fluorophenyl group attached to a vinyl group, which is in turn connected to the benzoxazole core. This specific chemical structure endows it with unique properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. Due to its complex structure and potential reactivity, it is essential to handle Benzoxazole, 2-[2-(4-fluorophenyl)ethenyl]- with care and follow proper safety protocols.

1493-41-0

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1493-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1493-41-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1493-41:
(6*1)+(5*4)+(4*9)+(3*3)+(2*4)+(1*1)=80
80 % 10 = 0
So 1493-41-0 is a valid CAS Registry Number.

1493-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(4-fluorophenyl)ethenyl]-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:1493-41-0 SDS

1493-41-0Downstream Products

1493-41-0Relevant academic research and scientific papers

Preparation method of 2-styrylbenzoxazole derivatives and application of 2-styrylbenzoxazole derivatives in anti-tumor effect

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Paragraph 0030-0031, (2017/06/15)

The invention discloses a structure and preparation method of 2-styrylbenzoxazole derivatives. 2-styrylbenzoxazole and different substituted aromatic aldehydes are taken as raw materials to react in one step under the anhydrous and oxygen-free conditions and the action of potassium tert-butoxide to generate 2-styrylbenzoxazole heterocyclic compounds. The preparation method has the advantages of being simple in reaction step, short in reaction time, good in selectivity and the like. In addition, the invention further provides research on application of an anti-tumor effect. The compounds 1, 2, 3 and 4 all show the certain bioactivity on in-vitro HepG2 cell proliferation inhibition, wherein the inhibition rate of the compound 1 on in-vitro HepG2 cell proliferation under the 100 micrometer concentration reaches 85.4%, and the inhibition rate of the compound 4 on in-vitro HepG2 cell proliferation under the 100 micrometer concentration reaches up to 93.4%.

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