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2-(4-Fluorophenyl)oxazole is a heterocyclic aromatic compound with the molecular formula C9H6FNO. It features an oxazole ring, which is a five-membered ring containing oxygen and nitrogen atoms, fused with a 4-fluorophenyl group. 2-(4-Fluorophenyl)oxazole is commonly utilized in organic synthesis and pharmaceutical research due to its potential biological activities and unique chemical properties.

885268-39-3

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885268-39-3 Usage

Uses

Used in Pharmaceutical Research and Development:
2-(4-Fluorophenyl)oxazole is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological effects. Its unique structure allows it to be a promising candidate in the development of new drugs with novel mechanisms of action.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(4-Fluorophenyl)oxazole serves as a valuable building block for the creation of complex organic molecules. Its reactivity and structural features make it suitable for the synthesis of a wide range of compounds with potential applications in various industries.
Used in Medicinal Chemistry:
2-(4-Fluorophenyl)oxazole is employed as a structural motif in medicinal chemistry to design and optimize drug candidates. Its presence in a molecule can modulate pharmacokinetic and pharmacodynamic properties, leading to improved drug efficacy and safety profiles.
Used in Agrochemicals:
2-(4-Fluorophenyl)oxazole may also find applications in the development of agrochemicals, such as pesticides and herbicides, due to its potential biological activities. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds while minimizing environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 885268-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,6 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 885268-39:
(8*8)+(7*8)+(6*5)+(5*2)+(4*6)+(3*8)+(2*3)+(1*9)=223
223 % 10 = 3
So 885268-39-3 is a valid CAS Registry Number.

885268-39-3SDS

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-(4-Fluorophenyl)oxazole

1.2 Other means of identification

Product number -
Other names 2-(4-fluorophenyl)-1,3-oxazole

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:885268-39-3 SDS

885268-39-3Relevant academic research and scientific papers

Orientation effects on C2(5)-C2?(5?) linked bioxazole isomers synthesized via regioselective and sequential C[sbnd]H arylation

Guo, Qiang,Tao, Li,Liu, Chuanqi,Zhao, Xiaoyun,Wan, Danyang,Zhang, Jincheng,Ai, Jianping,Li, Jie

supporting information, p. 425 - 428 (2020/06/17)

Bis(4-fluorophenyl) substituted oxazole (2,5-Oxz) and C2(5)-C2?(5?) linked bioxazole isomers (C2-C2?_BOxz, C2-C5?_BOxz and C5-C5?_BOxz) were concisely synthesized via palladium-catalyzed regioselective and sequential C[sbnd]H arylation in 1–3 reaction steps along with 20%–83% of total yields from oxazole and 4-bromofluorobenzene. The linking orientation plays a key role in the packing geometry and photophysical properties of C2-C2'_BOxz, C2-C5'_BOxz and C5-C5'_BOxz. These bioxazole isomers in solid state showed significant differences in photoluminescence quantum yields (PLQY) (0.33, 0.25 and 0.04, respectively), delayed fluorescence properties and powder X-ray diffraction (PXRD) patterns, suggesting the divergence in intermolecular interactions. The theoretically calculated gradient isosurfaces and complexation energies indicate the existence of intense π-π interactions between molecular layers, which are in good agreement with the variation trend of optical properties.

Warming Up to Oxazole: Noncryogenic Oxazole Metalation and Negishi Coupling Development

Calimsiz, Selcuk,Geier, Michael J.,Humphreys, Luke D.,Scott, Mark E.,Wang, Xiaotian

, p. 1776 - 1781 (2019/09/09)

This report details the development of several suitable noncryogenic metalation conditions for the synthesis of oxazole zincate. Subsequent rounds of high-throughput catalyst screening ultimately led to the identification of several suitable Pd sources th

PYRIDINE DERIVATIVES

-

Page/Page column 80; 81, (2013/04/13)

The present application provides novel pyridine compounds and pharmaceutically acceptable salts or prodrugs thereof. Also provided are methods for preparing these compounds. These compounds are useful in inhibiting CYP 17 activity by administering a therapeutically effective amount of one or more of the compounds to a patient. By doing so, these compounds are effective in treating conditions associated with CPY17 activity. A variety of conditions can be treated using these compounds and include diseases which are characterized by abnormal cellular proliferation. In one embodiment, the disease is cancer, such as prostate cancer.

Nickel-catalyzed synthesis of oxazoles via C-S activation

Lee, Kyoungsoo,Counceller, Carla M.,Stambuli, James P.

supporting information; experimental part, p. 1457 - 1559 (2009/08/08)

The synthesis of 2-substituted oxazoles is achieved via nickel-catalyzed cross-coupling reaction of 2-methylthio-oxazole and various organozinc reagents. An extension of this method is demonstrated with a chemoselective, one-pot synthesis of unsymmetrical

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