1459-49-0

Basic information

• Product Name: 1-(p-Nitrophenyl)adamantane
• Synonyms: 1-(p-Nitrophenyl)adamantane;MFCD00185797;p-(Adamantyl-1)nitrobenzene
• CAS NO: 1459-49-0
• Molecular Formula: C₁₆H₁₉NO₂
• Molecular Weight: 273.32696
• EINECS: -0
• Mol File: 1459-49-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 129-130℃
• Appearance: /
• Density: 1.224±0.06 g/cm3 (20 ºC 760 Torr)
• CAS DataBase Reference: 1-(p-Nitrophenyl)adamantane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(p-Nitrophenyl)adamantane(1459-49-0)
• EPA Substance Registry System: 1-(p-Nitrophenyl)adamantane(1459-49-0)

Safety Data

• Hazardous Substances Data: 1459-49-0(Hazardous Substances Data)

Usage

General Description

1-(p-Nitrophenyl)adamantane is a synthetic chemical compound that is derived from the combination of a nitrophenyl group and an adamantane core structure. It is commonly used in the field of organic and medicinal chemistry as a building block for constructing complex molecules. The compound's unique structure and reactivity make it a valuable starting material for the synthesis of various pharmaceuticals, agrochemicals, and other biologically active compounds. Its strong electron-withdrawing nitro group and rigid adamantane core impart specific properties and functionalities that are beneficial for the development of new drugs and materials. Additionally, 1-(p-Nitrophenyl)adamantane has been studied for its potential applications in organic electronics and materials science due to its interesting electronic and physical properties.

Upstream product

• 71-43-2 benzene 
• 768-90-1 1-Adamantyl bromide 
• 281-23-2 adamantane 
• 100-25-4 para-dinitrobenzene 
• 828-51-3 1-Adamantanecarboxylic acid 
• 780-68-7 1-phenyladamantane 

Downstream Products

• 940894-18-8 C₅₉H₅₇IN₂O₄ 
• 940894-16-6 3-(4-iodophenyl)-1-(4-nitrophenyl)adamantane 
• 940894-17-7 3-(4-iodophenyl)-1-(4-aminophenyl)adamantane 
• 61065-64-3 1-<4-Amino-phenyl>-3-brom-adamantan 
• 7164-55-8 ethyl 4-(adamantan-1-yl)benzoate 
• 7164-56-9 1-<4-Ethoxymethyl-phenyl>-adamantan 
• 7131-09-1 1-(4-(bromomethyl)phenyl)adamantane 
• 7131-08-0 (4-(adamantan-1-yl)phenyl)methanol 
• 7123-78-6 4-(adamant-1-yl)benzoic acid 
• 7123-76-4 3-(4-nitrophenyl)-1-adamantanecarboxylic acid 
• 7163-95-3 4-(adamantan-1-yl)benzonitrile 
• 15175-23-2 1-(4-nitrophenyl)-3-phenyladamantane 
• 68748-95-8 Trifluoro-acetic acid 3-(4-nitro-phenyl)-adamantan-1-yl ester 
• 94238-09-2 1-Nitrooxy-3-(4-nitro-phenyl)-adamantane 

Relevant articles and documents

Modes of Micromolar Host-Guest Binding of β-Cyclodextrin Complexes Revealed by NMR Spectroscopy in Salt Water

Multitopic supramolecular guests with finely tuned affinities toward widely explored cucurbit[n]urils (CBs) and cyclodextrins (CDs) have been recently designed and tested as functional components of advanced supramolecular systems. We employed various spa

REACTION OF MONOFUNCTIONAL SUBSTITUTED ADAMANTANES WITH NITRIC ACID AND ITS MIXTURES

In the reaction of monofunctional substituted adamantanes with nitric acid and its mixtures the main reaction products are the nitrates of adamantanol, formed either as a result of substitution of the functional groups or as a result of substitution of a hydrogen atom at a tertiary carbon atom.