Yahoo Web Search

Search results

1. Images

   • 
   • 
   • 
   • 

   View all

2. pubchem.ncbi.nlm.nih.gov › 1-phenylcyclohexylamine1-Phenylcyclohexylamine | C12H17N | CID 31862 - PubChem

   pubchem.ncbi.nlm.nih.gov › 1-phenylcyclohexylamine

   1-Phenylcyclohexylamine | C12H17N | CID 31862 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

3. webbook.nist.gov › cgi › cbookN-Phenylcyclohexylamine - NIST Chemistry WebBook

   webbook.nist.gov › cgi › cbook

   • Cached

   Feb 6, 2010 · N-Phenylcyclohexylamine. Formula: C 12 H 17 N. Molecular weight: 175.2701. IUPAC Standard InChI: InChI=1S/C12H17N/c1-3-7-11 (8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2. Copy Sheet of paper on top of another sheet.

4. People also ask

   How is benzene converted to phenylamine?

   • The benzene is first converted to nitrobenzene which is in turn reduced to phenylamine. Benzene is nitrated by replacing one of the hydrogen atoms on the benzene ring by a nitro group, NO 2. The benzene is treated with a mixture of concentrated nitric acid and concentrated sulphuric acid at a temperature not exceeding 50°C.

   Preparation of Phenylamine Compounds - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Phenylamine_and_Diazonium_Compounds/Preparation_of_Phenylamine_Compounds

   See all results for this question

   How does phenylamine react with nitrobenzene?

   • Under the acidic conditions, rather than getting phenylamine directly, you instead get phenylammonium ions formed. The lone pair on the nitrogen in the phenylamine picks up a hydrogen ion from the acid. The electron-half-equation for this reaction is: The nitrobenzene has been reduced by gaining electrons in the presence of the acid.

   Preparation of Phenylamine Compounds - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Phenylamine_and_Diazonium_Compounds/Preparation_of_Phenylamine_Compounds

   See all results for this question

   What happens when sodium hydroxide solution is added to phenylamine?

   • Sodium hydroxide solution is added to the product of the first stage of the reaction. The phenylamine is formed together with a complicated mixture of tin compounds from reactions between the sodium hydroxide solution and the complex tin ions formed during the first stage. The phenylamine is finally separated from this mixture.

   Preparation of Phenylamine Compounds - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Phenylamine_and_Diazonium_Compounds/Preparation_of_Phenylamine_Compounds

   See all results for this question

   Which lone pair picks up a hydrogen ion from a phenylamine?

   • The lone pair on the nitrogen in the phenylamine picks up a hydrogen ion from the acid. The electron-half-equation for this reaction is: The nitrobenzene has been reduced by gaining electrons in the presence of the acid. The electrons come from the tin, which forms both tin (II) and tin (IV) ions. Sn → Sn2+ + 2e− (2) (2) S n → S n 2 + + 2 e −

   Preparation of Phenylamine Compounds - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Phenylamine_and_Diazonium_Compounds/Preparation_of_Phenylamine_Compounds

   See all results for this question

5. webbook.nist.gov › cgi › cbookN-Phenylcyclohexylamine - NIST Chemistry WebBook

   webbook.nist.gov › cgi › cbook

   • Cached

   For Zoom; 1.) Enter the desired X axis range (e.g., 100, 200) 2.) Check here for automatic Y scaling 3.) Press here to zoom

   • Date: 1959/09/22
   • Origin: MONSANTO (J. FREEMAN)

   • Name(s): N-cyclohexylanilineN-cyclohexyl-N-phenylamine
   • Source reference: COBLENTZ NO. 08474

6. chem.libretexts.org › Bookshelves › OrganicPreparation of Phenylamine Compounds - Chemistry LibreTexts

   chem.libretexts.org › Bookshelves › Organic

   • Cached

   Jan 23, 2023 · Stage 1: conversion of nitrobenzene into phenylammonium ions. Nitrobenzene is reduced to phenylammonium ions using a mixture of tin and concentrated hydrochloric acid. The mixture is heated under reflux in a boiling water bath for about half an hour. Under the acidic conditions, rather than getting phenylamine directly, you instead get ...

7. go.drugbank.com › drugs › DB015061-Phenylcyclohexylamine: Uses, Interactions, Mechanism of ...

   go.drugbank.com › drugs › DB01506

   • Cached

   • Identification
   • Pharmacology
   • Interactions
   • Chemical Identifiers
   • Pharmacoeconomics
   • Properties

   Generic Name

   1. 1-Phenylcyclohexylamine

   DrugBank Accession Number

   1. DB01506

   Background

   1. Not Available

   See full list on go.drugbank.com

   Indication

   1. Not AvailableReduce drug development failure ratesBuild, train, & validate machine-learning models with evidence-based and structured datasets.See howsee_moreBuild, train, & validate predictive machine-learning models with structured datasets.See how

   Contraindications & Blackbox Warnings

   1. Prevent Adverse Drug Events TodayTap into our Clinical API for life-saving information on contraindications & blackbox warnings, population restrictions, harmful risks, & more.Learn moresee_moreAvoid life-threatening adverse drug events with our Clinical APILearn more

   Pharmacodynamics

   1. Not Available

   See full list on go.drugbank.com

   Drug Interactions information

   1. This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist. Not Available

   Food Interactions

   1. Not Available

   See full list on go.drugbank.com

   UNII

   1. HBO2D49I2S

   CAS number

   1. 2201-24-3

   InChI Key

   1. RGZGRPPQZUQUCR-UHFFFAOYSA-N

   See full list on go.drugbank.com

   Manufacturers

   1. Not Available

   Packagers

   1. Not Available

   Dosage Forms

   1. Not Available

   See full list on go.drugbank.com

   State

   1. Solid

   Experimental Properties

   1. Not Available

   See full list on go.drugbank.com

8. pubs.acs.org › doi › 101-Phenylcycloalkylamine derivatives. II. Synthesis and ...

   pubs.acs.org › doi › 10

   An expedient synthesis of high specific activity tritium labelled 4‐fluoro‐1‐[1‐(2‐thienyl)]cyclohexylpiperidine ([ 3 H]FTCP), a ligand for further characterization of the phencyclidine/NMDA receptor complex.

9. pubchem.ncbi.nlm.nih.gov › compound › 11-Phenylcyclohexylamine hydrochloride | C12H18ClN | CID ...

   pubchem.ncbi.nlm.nih.gov › compound › 1

   1-Phenylcyclohexylamine hydrochloride | C12H18ClN | CID 200391 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.