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

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

Uses

Used in Organic and Medicinal Chemistry:
1-(p-Nitrophenyl)adamantane serves as a valuable starting material for constructing complex molecules in organic and medicinal chemistry. Its unique structure and reactivity facilitate the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and materials.
Used in Organic Electronics and Materials Science:
Due to its interesting electronic and physical properties, 1-(p-Nitrophenyl)adamantane has been studied for potential applications in organic electronics and materials science. Its properties may be harnessed to create innovative materials with enhanced performance characteristics for use in various electronic devices and systems.

Upstream product

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

Downstream Products

• 54451-85-3 3-(p-Nitro-phenyl)-1-chlor-adamantan 
• 1459-48-9 4-(tricyclo[3.3.1.1^3,7]dec-1-yl)aniline 
• 7163-93-1 3-Brom-1-<4-nitro-phenyl>-adamantan 
• 94238-09-2 1-Nitrooxy-3-(4-nitro-phenyl)-adamantane 
• 68748-95-8 Trifluoro-acetic acid 3-(4-nitro-phenyl)-adamantan-1-yl ester 
• 15175-23-2 1-(4-nitrophenyl)-3-phenyladamantane 
• 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 

Relevant articles and documents

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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

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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.

Hypobetalipoproteinemic agents. II. Compounds related to 4-(1- adamantyloxy)aniline

While the previously used displacement reaction of sodium 1-adamantyl oxide on 4-fluoronitrobenzene was applicable to the preparation of 4-(1-adamantyloxy) aniline and several related compounds, certain derivatives were not easily accessible by this route