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833-50-1

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833-50-1 Usage

Description

2-Phenylbenzoxazole is a hydrophobic fluorophore found in fluorescent molecular sensors AS1-3. It is a derivative of benzoxazole, a heterocyclic compound consisting of a benzene ring fused to an oxazole ring. The presence of a phenyl group attached to the benzene ring gives 2-Phenylbenzoxazole unique properties and potential applications in various fields.

Uses

Used in Fluorescent Molecular Sensors:
2-Phenylbenzoxazole is used as a hydrophobic fluorophore in fluorescent molecular sensors, such as AS1-3. Its unique photophysical properties, including high fluorescence quantum yield and photostability, make it suitable for detecting and monitoring various analytes in biological and environmental systems.
Used in Chemical Synthesis:
2-Phenylbenzoxazole and its derivatives have been studied for their synthesis and potential applications in various fields. The synthesis of new series of 5-benzamidoand 5-phenylacetamido-substituted-2-phenylbenzoxazole derivatives has been investigated, which may lead to the development of new compounds with specific properties and uses.
Used in Microbiological Applications:
The microbiological activity of 2-Phenylbenzoxazole and its derivatives has been studied, indicating their potential use in antimicrobial applications. These compounds may exhibit inhibitory effects against certain microorganisms, making them useful in the development of new antimicrobial agents.

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 12, p. 1135, 1964Chemistry Letters, 20, p. 1275, 1991Tetrahedron, 53, p. 457, 1997 DOI: 10.1016/S0040-4020(96)01009-5

Check Digit Verification of cas no

The CAS Registry Mumber 833-50-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 833-50:
(5*8)+(4*3)+(3*3)+(2*5)+(1*0)=71
71 % 10 = 1
So 833-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H

833-50-1 Well-known Company Product Price

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  • Alfa Aesar

  • (B24906)  2-Phenylbenzoxazole, 99%   

  • 833-50-1

  • 1g

  • 549.0CNY

  • Detail
  • Alfa Aesar

  • (B24906)  2-Phenylbenzoxazole, 99%   

  • 833-50-1

  • 5g

  • 1972.0CNY

  • Detail
  • Alfa Aesar

  • (B24906)  2-Phenylbenzoxazole, 99%   

  • 833-50-1

  • 25g

  • 7711.0CNY

  • Detail
  • Aldrich

  • (310565)  2-Phenylbenzoxazole  99%

  • 833-50-1

  • 310565-5G

  • 2,060.37CNY

  • Detail

833-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Phenylbenzoxazole

1.2 Other means of identification

Product number -
Other names 2-phenyl-1,3-benzoxazole

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:833-50-1 SDS

833-50-1Relevant articles and documents

-

McEvoy,F.J.,Allen,G.R.

, p. 1183 - 1185 (1970)

-

A multistep flow process for the synthesis of highly functionalized benzoxazoles

Sedelmeier, Joerg,Lima, Fabio,Litzler, Alain,Martin, Benjamin,Venturoni, Francesco

, p. 5546 - 5549 (2013)

An efficient and scalable transformation of 3-halo-N-acyl anilines to the corresponding benzoxazoles within a continuous flow reactor is reported. This transformation proceeds via base-mediated deprotonation, ortho-lithiation, and intramolecular cyclization to provide unstable lithiated benzoxazole moieties. The subsequent in-line electrophilic quench results in the formation of substituted benzoxazoles in high yield and quality. Continuous flow technology allowed for accurate temperature control and immediate in-line quench while minimizing the hold-up time for the unstable lithiated intermediates thereby minimizing associated byproduct formation.

-

Higgins,Marvel

, p. 171,176 (1970)

-

-

Galatis

, p. 1967 (1948)

-

Iron(III) Chloride Mediated para-Selective C-H Functionalization: Access to C5-Chloro and C5,C7-Dichloro/Dianisyl Substituted 2-Arylbenzoxazoles

Panda, Niranjan,Sahoo, Kanchanbala

supporting information, (2022/02/03)

Iron(III) chloride mediated para-selective C?H chlorination and subsequent annulation of 2-amidophenol to synthesize C5- and C5, C7-chlorinated benzoxazoles was developed. Further, the oxidative cross-dehydrogenative coupling of amidophenol with anisole b

Heterocyclic reaction inducted by Br?nsted–Lewis dual acidic Hf-MOF under microwave irradiation

Nguyen, Linh Ho Thuy,Nguyen, Trang Thi Thu,Dang, Minh-Huy Dinh,Tran, Phuong Hoang,Doan, Tan Le Hoang

, (2020/11/24)

Use of green chemistry and alternative strategies has been explored to prepare diverse organic derivatives. The combination between heterogeneous catalyst, environmentally benign reaction and high-yielding methods is gaining momentum. Herein, a defective 6-connected Hf-MOF, named Hf-BTC, was efficiently synthesized and characterized for the heterogeneous catalysis under microwave irradiation. The MOF features including structural defect, porosity, acidity, and stability was analyzed by powder X-ray diffraction, N2 sorption isotherms, acid-base titration, and thermal gravimetric analysis. In the catalytic studies, the Br?nsted-Lewis dual acidic Hf-BTC was efficiently applied for the synthesis of the heterocyclic compounds via the microwave-assisted cycloaddition and condensation reactions. The reactions proceeded smoothly in the presence of the Hf-MOF with a broad scope of substrates provided the expected products in high to excellent yields (up to 99 %) for few minutes and the catalyst could be easily recycle over many consecutive reactions without loss of its reactivity and structure.

An efficient rapid synthesis of benzoxazoles and benzothiazoles using pma.Sio2 at room temperature under heterogeneous conditions

Sudhakar, Chithaluri,Shekhar, Vanam,Shyamsunder, Manchi,Suryakumari, Adurthi,Manojkumar, Vala

, p. 583 - 587 (2021/09/30)

Treatment of 2-aminophenol (or 2-aminothiophenol) with aromatic aldehydes in the presence of phosphomolybdic acid on silica at room temperature affords the corresponding benzoxazoles (or benzothiazoles) in excellent yields (88-96%) under heterogeneous conditions. Benzoxazoles and benzothiazoles are formed in less than 10 min.

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