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2-(4-BIPHENYL)-5-PHENYLOXAZOLE 98% is a high-purity specialized chemical compound belonging to the oxazole class, which features a five-membered aromatic ring composed of three carbon atoms, one oxygen atom, and one nitrogen atom. Its unique chemical structure, including a biphenyl group and a phenyl group, contributes to its distinct chemical properties and potential applications.

852-37-9

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852-37-9 Usage

Uses

Used in Research and Industrial Settings:
2-(4-BIPHENYL)-5-PHENYLOXAZOLE 98% is used as a research and industrial chemical for its reactivity and specific behaviors under certain conditions, such as emitting fluorescence. Its applications are diverse and depend on the requirements of the project or industry.

Check Digit Verification of cas no

The CAS Registry Mumber 852-37-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 852-37:
(5*8)+(4*5)+(3*2)+(2*3)+(1*7)=79
79 % 10 = 9
So 852-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H15NO/c1-3-7-16(8-4-1)17-11-13-19(14-12-17)21-22-15-20(23-21)18-9-5-2-6-10-18/h1-15H

852-37-9 Well-known Company Product Price

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  • Aldrich

  • (216984)  2-(4-Biphenyl)-5-phenyloxazole  98%

  • 852-37-9

  • 216984-1G

  • 470.34CNY

  • Detail

852-37-9SDS

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 5-phenyl-2-(4-phenylphenyl)-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2-(4-biphenyl)-5-phenyloxazole

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:852-37-9 SDS

852-37-9Relevant academic research and scientific papers

Divergent Conversion of N-Acyl-isoxazol-5(2 H)-ones to Oxazoles and 1,3-Oxazin-6-ones Using Photoredox Catalysis

Mei, Mingjing,Anand, Devireddy,Zhou, Lei

supporting information, p. 3548 - 3553 (2019/05/24)

The fragmentation of N-acyl-isoxazol-5-ones using visible light photoredox catalysis has been disclosed. The catalyst-controlled divergent mechanisms, namely the oxidative and reductive quenching catalytic cycle, are utilized. Various oxazoles and 1,3-oxazin-6-ones are selectively obtained from the same isoxazol-5-one skeleton under mild conditions.

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