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

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

   Oct 14, 2021 · 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

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   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. IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N.

4. People also ask

   Does phenylamine react with ethanoyl chloride?

   • We'll take ethanoyl chloride as a typical acyl chloride, and ethanoic anhydride as a typical acid anhydride. The important product of the reaction of phenylamine with either of these is the same. Phenylamine reacts vigorously in the cold with ethanoyl chloride to give a mixture of solid products - ideally white, but usually stained brownish.

   Reactions of Phenylamine as a Primary Amine - Chemistry LibreTexts

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

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   How does phenylamine react with hydrochloric acid?

   • Phenylamine reacts with acids like hydrochloric acid in exactly the same way as any other amine. Despite the fact that the phenylamine is only a very weak base, with a strong acid like hydrochloric acid the reaction is completely straightforward. Phenylamine is only very slightly soluble in water, but dissolves freely in dilute hydrochloric acid.

   Reactions of Phenylamine as a Primary Amine - Chemistry LibreTexts

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

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   What is cyclohexylamine?

   • ?) Cyclohexylamine is an organic compound, belonging to the aliphatic amine class. It is a colorless liquid, although, like many amines, samples are often colored due to contaminants. It has a fishy odor and is miscible with water.

   Cyclohexylamine - Wikipedia

   en.wikipedia.org/wiki/Cyclohexylamine

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   How does bromoethane react with phenylamine?

   • Taking bromoethane as a typical halogenoalkane, the reaction with phenylamine happens in the same series of complicated steps as with any other amine. We'll just look at the first step. On heating, the bromoethane and phenylamine react to give a mixture of a salt of a secondary amine and some free secondary amine.

   Reactions of Phenylamine as a Primary Amine - Chemistry LibreTexts

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

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

   webbook.nist.gov › cgi › cbook

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   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. en.wikipedia.org › wiki › CyclohexylamineCyclohexylamine - Wikipedia

   en.wikipedia.org › wiki › Cyclohexylamine

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   Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide -based reagents used as accelerators for vulcanization. It is a building block for pharmaceuticals (e.g., mucolytics, analgesics, and bronchodilators ).

   • Chemical formula: C₆H₁₃N
   • Molar mass: 99.17

   • Melting point: −17.7 °C (0.1 °F; 255.5 K)
   • Solubility in water: Miscible

7. www.chem.ucalgary.ca › courses › 353Chem 353 Final 2003 : Synthesis - Faculty of Science

   www.chem.ucalgary.ca › courses › 353

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   Chem 353 Final 2003 : Synthesis. Part 9: SYNTHESIS. The schemes below give possible syntheses of the targets. There are of course other variations. The first part for each compound gives a "retro-synthesis", the "plan" and then the forward synthesis with reagents is given. Red arrows try to show carbon-carbon bond forming reactions, blue arrows ...

8. chem.libretexts.org › Bookshelves › OrganicReactions of Phenylamine as a Primary Amine - Chemistry ...

   chem.libretexts.org › Bookshelves › Organic

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   Jan 23, 2023 · Truro School in Cornwall. This page looks at reactions of phenylamine (also known as aniline or aminobenzene) where it behaves as a fairly straightforward primary amine. It explains why phenylamine is a weaker base than other primary amines, and summarises its reactions with acyl chlorides (acid chlorides), acid anhydrides and halogenoalkanes ...

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.