2-(4-Nitrophenoxy)naphthalene, with the CAS number 71311-82-5, is an organic compound characterized by its naphthalene backbone substituted with a 4-nitrophenoxy group. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the presence of both naphthalene and phenolic structures. The nitro group (-NO2) attached to the phenoxy moiety contributes to its electron-withdrawing characteristics, which can influence its reactivity and solubility in various solvents. It is often used in organic synthesis and may serve as an intermediate in the production of dyes, pharmaceuticals, or other chemical compounds. The presence of the nitro group also suggests potential applications in materials science, particularly in the development of functional materials or as a precursor for further chemical modifications. Safety data should be consulted for handling, as nitro compounds can be sensitive and may pose health risks.

2-(4-nitrophenoxy)naphthalene

71311-82-5: 2-Naphthyl 4-nitrophenyl ether, Naphthalen-2-Yl 4-Nitrophenyl Ether, Naphthalene, 2-(4-Nitrophenoxy)-

2-(4-Nitrophenoxy)Naphthalene

2-(4-Nitrophenoxy)naphthalene can be used as a catalyst in the transformation of ethers to their corresponding hydrocarbons. This is an aerobic reaction, which yields high yields. The coupling reaction is catalyzed by a diaryliodonium salt and 2-(4-nitrophenoxy)naphthalene. The use of this efficient catalyst system can lead to the formation of phenols or aryl iodides from diaryliodonium salts and aryl halides.

CAS 71311-82-5: 2-(4-nitrophenoxy)naphthalene

2-(4-Nitrophenoxy)Naphthalene

Ref: 54-OR1025003

2-(4-Nitrophenoxy)naphthalene

Ref: 3D-WCA31182

2-(4-nitrophenoxy)naphthalene

Ref: IN-DA003EXD

2-(4-Nitrophenoxy)naphthalene

Ref: 3B-N0807

2-(4-Nitrophenoxy)naphthalene

Ref: 10-F775628