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92148-95-3

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92148-95-3 Usage

Description

N-(4-Methoxyphenyl)benzo[d]oxazol-2-aMine is a chemical compound with the molecular formula C14H11NO2. It is a derivative of benzodioxazoles and contains a benzene and oxazole ring. N-(4-Methoxyphenyl)benzo[d]oxazol-2-aMine is known for its fluorescent properties, which make it useful for various applications in research and development.

Uses

Used in Research and Development:
N-(4-Methoxyphenyl)benzo[d]oxazol-2-aMine is used as a fluorescent labeling agent for imaging applications in research and development. Its fluorescent properties allow for the tracking and visualization of specific molecules or cellular structures, aiding in the study of biological processes and mechanisms.
Used as a Biological Probe:
Due to its unique structure and properties, N-(4-Methoxyphenyl)benzo[d]oxazol-2-aMine is used as a biological probe in the study of molecular interactions and the development of new pharmaceuticals. Its ability to bind to specific targets makes it a valuable tool in drug discovery and the investigation of biological systems.
Used in Pharmaceutical Development:
N-(4-Methoxyphenyl)benzo[d]oxazol-2-aMine has been studied for its potential use in the development of pharmaceuticals. Its unique structure and properties may contribute to the creation of new drugs with specific therapeutic effects.
Used in Organic Synthesis:
N-(4-Methoxyphenyl)benzo[d]oxazol-2-aMine is also utilized in the synthesis of various organic compounds due to its unique structure and properties. Its versatility in chemical reactions makes it an important building block in the creation of new organic molecules for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 92148-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,4 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92148-95:
(7*9)+(6*2)+(5*1)+(4*4)+(3*8)+(2*9)+(1*5)=143
143 % 10 = 3
So 92148-95-3 is a valid CAS Registry Number.

92148-95-3Downstream Products

92148-95-3Relevant articles and documents

Microwave-assisted hydrogen peroxide-mediated synthesis of benzoxazoles and related heterocycles via cyclodesulfurization

Kadagathur, Manasa,Sigalapalli, Dilep Kumar,Patra, Sandip,Tangellamudi, Neelima D.

supporting information, p. 2213 - 2224 (2021/05/26)

A novel approach has been developed to construct benzoxazoles and similar N- and S-containing heterocycles from their corresponding isothiocyanates and o-substituted anilines via cyclodesulfurization. The reaction was found to proceed via in situ formatio

Electrochemical NaI/NaCl-mediated one-pot synthesis of 2-aminobenzoxazoles in aqueous mediaviatandem addition-cyclization

Huynh, Thao Nguyen Thanh,Koguchi, Shinichi,Rerkrachaneekorn, Tanawat,Sukwattanasinitt, Mongkol,Tankam, Theeranon,Wacharasindhu, Sumrit

supporting information, p. 5189 - 5194 (2021/07/29)

An electrochemical synthesis of 2-aminobenzoxazoles from 2-aminophenols and isothiocyanates was successfully developed in a one-pot fashion. Using inexpensive and widely available NaI and NaCl co-operatively in catalytic amounts, our electrosynthesis approach provided various 2-aminobenzoxazole products in moderate to high yields in an open-flask type undivided cell without using any external supporting electrolyte and base. The protocol can be applied to the synthesis of 2-aminobenzothiazoles from the corresponding 2-thiophenols in moderate yields. This protocol has many benefits. It is metal-free and highly scalable and uses inexpensive mediators and EtOH/water as an environmentally friendly solvent under mild conditions.

Cobalt-Catalyzed Aerobic Oxidative Cyclization of 2-Aminophenols with Isonitriles: 2-Aminophenol Enabled O2 Activation by Cobalt(II)

Liu, Jiaqi,Hoover, Jessica M.

supporting information, p. 4510 - 4514 (2019/06/27)

An aerobic cobalt-catalyzed oxidative cyclization of 2-aminophenols and isonitriles is reported. These additive-free conditions furnish a variety of substituted 2-aminobenzoxazoles in moderate to excellent yields. A series of control experiments and spect

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