| 词条 | N,N-Dimethyl-1-naphthylamine |
| 释义 |
| Name = N,N-Dimethyl-1-naphthylamine | ImageFile = N,N-dimethyl-1-naphthylamine-2D-skeletal-CH3.png | ImageSize = 140px | ImageName = skeletal formula | ImageFile1 = N,N-Dimethyl-1-naphtylamine ampoule.jpg | ImageSize1 = 265px | ImageName1 = Ampoule with substance. | IUPACName = | OtherNames = N,N-dimethylnaphthalen-1-amine |Section1={{Chembox Identifiers | CASNo = 86-56-6 | PubChem = 24893807 | ChemSpiderID = 6587 | SMILES = c1cccc2cccc(N(C)C)c12 | InChI = 1/C12H13N/c1-13(2)12-9-5-7-10-6-3-4-8-11(10)12/h3-9H,1-2H3 | InChIKey = AJUXDFHPVZQOGF-UHFFFAOYAQ |Section2={{Chembox Properties | C=12 | H=13 | N=1 | Density = 1.042 g/cm3 at 25 °C | MeltingPt = | BoilingPtC = 139 to 140 | BoilingPt_notes = at 13 mmHg | Properties_ref = [1][2] |Section3={{Chembox Related | OtherCompounds = 1-naphthylamine 1-naphthol naphthalene aniline dimethylaniline Proton Sponge }}N,N-Dimethyl-1-naphthylamine is an aromatic amine. It is formally derived from 1-naphthylamine by replacing the hydrogen atoms on the amino group with methyl groups. N,N-Dimethyl-1-naphthylamine is used in the nitrate reductase test to form a red precipitate of Prontosil by reacting with a nitrite-sulfanilic acid complex.[3] References1. ^{{ cite web | url = http://www.chemspider.com/Chemical-Structure.6587.html | title = N,N-dimethylnaphthalen-1-amine | publisher = ChemSpider | accessdate = 15 April 2010 }} {{DEFAULTSORT:Dimethyl-1-naphthylamine, N,N-}}{{amine-stub}}2. ^{{ cite web | url = http://www.sigmaaldrich.com/catalog/product/sial/d4011 | title = D4011 N,N-Dimethyl-1-naphthylamine, ≥98.0% (GC) | publisher = Sigma-Aldrich | accessdate = 15 April 2010 }} 3. ^{{ cite web | title = 73426 (Fluka) Nitrate Reduction Test | url = http://www.sigmaaldrich.com/catalog/product/fluka/73426 | publisher = Sigma-Aldrich | accessdate= 15 April 2010 }} 1 : Naphthylamines |
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