54564-31-7

Basic information

• Product Name: 2-nitroadamantane
• Synonyms: 2-nitroadamantane
• CAS NO: 54564-31-7
• Molecular Formula: C10H15NO2
• Molecular Weight: 181.231600
• Mol File: 54564-31-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 285.9 °C at 760 mmHg
• Flash Point: 128.5 °C
• Appearance: /
• Density: 1.18 g/cm³
• Vapor Pressure: 0.00272mmHg at 25°C
• Refractive Index: 1.541
• CAS DataBase Reference: 2-nitroadamantane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-nitroadamantane(54564-31-7)
• EPA Substance Registry System: 2-nitroadamantane(54564-31-7)

Safety Data

• Hazardous Substances Data: 54564-31-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H15NO2/c12-11(13)10-8-2-6-1-7(4-8)5-9(10)3-6/h6-10H,1-5H2

Upstream product

• 13074-39-0 N-(2-adamantyl)amine 
• 40854-02-2 2-bromo-2-nitro-adamantane 
• 4500-12-3 2-adamantanone oxime 

Downstream Products

• 88381-75-3 2,2-dinitroadamantane 
• 33673-34-6 2-chloro-2-nitrosoadamantane 

Relevant articles and documents

ADAMANTANE ANALOGS

Provided are compounds that are capable of modulating the activity of the influenza A virus via interaction with the M2 transmembrane protein. Also provided are methods for treating an influenza A-affected disease state or infection comprising administering a composition comprising one or more compounds that have been identified as being capable of interaction with the M2 protein.

Fluorination of Nitro Compounds with Acetyl Hypofluorite

Various types of nitro derivatives are fluorinated to form the CFNO2 moiety in very good yields using acetyl hypofluorite (AcOF).The corresponding nitro anion, preferably prepared with NaOMe, is added quickly to a cold (-75 deg C) CFCl3 solution of AcOF,

Synthesis by the S(RN)1 reaction of a new series of imidazo[1,2-a]pyridine derivatives with pharmacological potentialities

The study of S(RN)1 reaction between 2-chloromethyl-3-nitroimidazo[1,2-a] pyridine and 2-nitropropane salts has been extended to various aliphatic, cyclic and heterocyclic nitronate anions. From C-alkylation products, base-promoted nitrous acid elimination afforded new potential pharmacological derivatives with a trisubstituted double bond at the 2 position.