77635-08-6

Basic information

• Product Name: 1-Naphthalen-t-amine,N-hydroxy-(9CI)
• Synonyms: 1-Naphthalen-t-amine,N-hydroxy-(9CI)
• CAS NO: 77635-08-6
• Molecular Formula: C10H8NOT
• Molecular Weight: 159.19
• Product Categories: BIPHENYL
• Mol File: 77635-08-6.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Naphthalen-t-amine,N-hydroxy-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalen-t-amine,N-hydroxy-(9CI)(77635-08-6)
• EPA Substance Registry System: 1-Naphthalen-t-amine,N-hydroxy-(9CI)(77635-08-6)

Safety Data

• Hazardous Substances Data: 77635-08-6(Hazardous Substances Data)

Usage

Description

1-Naphthalen-t-amine,N-hydroxy-(9CI), also known as 1-Naphthylamine N-oxide, is a chemical compound with the molecular formula C10H9NO. It is an amine, which is a nitrogen-containing organic molecule, that features a naphthalene ring structure. The N-hydroxy group in its chemical name signifies the presence of a hydroxyl (OH) group attached to the nitrogen atom. 1-Naphthalen-t-amine,N-hydroxy-(9CI) may have various applications and properties, but specific information about its uses and characteristics would need to be obtained from reliable sources.

Uses

1-Naphthalen-t-amine,N-hydroxy-(9CI) may be used in different industries and applications, although the provided materials do not specify any particular use. To determine its applications, one would need to consult scientific literature, patents, or other reliable sources that detail its properties and potential uses. If such information becomes available, the applications can be listed as follows:
Used in [Application Industry]:
1-Naphthalen-t-amine,N-hydroxy-(9CI) is used as [application type] for [application reason].

Upstream product

• 86-57-7 1-Nitronaphthalene 

Downstream Products

• 102543-55-5 N,O-dibenzoyl-N-[1]naphthyl-hydroxylamine 
• 72771-51-8 1-benzamido-2-naphthol 
• 80156-61-2 N-(guanin-C⁸-yl)-1-naphthylamine 
• 1018810-42-8 C₂₅H₂₄N₂O₄ 
• 1018810-43-9 C₂₈H₂₈N₂O₄ 
• 85-12-1 N-(4-hydroxy-1-naphthalenyl)acetamide 

Relevant articles and documents

Azo bond formation on metal surfaces

The formation of azo compounds via redox cross-coupling of nitroarenes and arylamines, challenging in solution phase chemistry, is achieved by on-surface chemistry. Reaction products are analyzed with a cryogenic scanning tunneling microscope (STM) and X-ray photoelectron spectroscopy (XPS). By using well-designed precursors containing both an amino and a nitro functionality, azo polymers are prepared on surface via highly efficient nitro-amino cross-coupling. Experiments conducted on other substrates and surface orientations reveal that the metal surface has a significant effect on the reaction efficiency. The reaction was further found to proceed from partially oxidized/reduced precursors in dimerization reactions, shedding light on the mechanism that was studied by DFT calculations.

Practical bromination of arylhydroxylamines with SOBr2 towards ortho-bromo-anilides

A facile approach for synthesizing ortho-bromoanilides from readily available aryhydroxylamines and thionyl bromide is demonstrated in this work. Mild reaction conditions and broad scope of substrates ranging from heterocyclic structures to pharmaceutics-potential motifs are used in the reactions of this paper. Efficient bromination of ortho C–H bonds of the aryhydroxylamines has been achieved. Ortho-bromoanilide products were obtained in good to excellent yields, and model scaled-up reactions of this synthetic approach are shown in this work.

A general and scalable synthesis of polysubstituted indoles

A consecutive 2-step synthesis of N-unprotected polysubstituted indoles bearing an electron-withdrawing group at the C-3 position from readily available nitroarenes is reported. The protocol is based on the [3,3]-sigmatropic rearrangement of N-oxyenamines generated by the DABCO-catalyzed reaction of N-arylhydroxylamines and conjugated terminal alkynes, and delivers indoles endowed with a wide array of substitution patterns and topologies.