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391-07-1

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391-07-1 Usage

Oxazole derivative

A five-membered heterocyclic ring containing one oxygen and one nitrogen atom.

Usage

Organic synthesis, medicinal chemistry (building block for the synthesis of biologically active compounds), pharmaceuticals, agrochemicals, and material science.

Unique structure and properties

Potential applications in various fields due to its specific chemical structure and characteristics.

Fluorescence probe

Utilized in analytical chemistry and bioimaging studies.

Aromatic and heterocyclic nature

Offers versatility for the development of new drugs and molecular probes.

Check Digit Verification of cas no

The CAS Registry Mumber 391-07-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 391-07:
(5*3)+(4*9)+(3*1)+(2*0)+(1*7)=61
61 % 10 = 1
So 391-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H10FNO/c16-13-9-5-4-8-12(13)15-17-10-14(18-15)11-6-2-1-3-7-11/h1-10H

391-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-fluorophenyl)-5-phenyl-1,3-oxazole

1.2 Other means of identification

Product number -
Other names oxazole,2-(2-fluorophenyl)-5-phenyl

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:391-07-1 SDS

391-07-1Downstream Products

391-07-1Relevant articles and documents

Synthesis of 2,5-disubstituted oxazoles: Via cobalt(III)-catalyzed cross-coupling of N -pivaloyloxyamides and alkynes

Yu, Xiaolong,Chen, Kehao,Wang, Qi,Zhang, Wenjing,Zhu, Jin

, p. 1197 - 1200 (2018/02/09)

An efficient synthesis of 2,5-disubstituted oxazoles via Co(iii) catalysis is described herein. The synthesis is achieved under mild conditions through [3+2] cycloaddition of N-pivaloyloxyamides and alkynes. The reaction operates through an internal oxidation pathway and features a very broad substrate scope. The one-step synthesis of natural products such as texamine and balsoxin has been demonstrated via this protocol.

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