2- methanamine

Chloro-N-[2,6-dinitro-4-(trifluoromethyl)-phenyl]-N-ethyl-6-fluorbenzenene- methanamine [62924-70-3]... 

Chemicai Name 4,5-Dihydro-N-phenyl-N-(phenylmethyl)-1 H-imidazole-2-methanamine... 

Chemical Name N-Methyl-9,10-ethanoanthracene-9(10H)-methanamine Common Name -... 

Dimethylamine (8) Methanamine, N-methyl- (9) (124-40-3) Methyl cyclohexanecarboxylate Cyclohexanecarboxylic acid, methyl ester (8, 9) (4630-82-4)... 

Cationic surfactants contain a positively charged headgroup and are typically used as conditioners to improve hair manageability and reduce static. Cationic surfactants are especially irritating to eyes when used in high concentrations but are safe and useful in low amounts. Quatemium-15 (chloroallyl methanamine chloride, Fig. 7.9.4) is a cationic surfactant included in shampoo formulations... 

Figure 7.9.4 The cationic surfactant quatemium-15 (chloroallyl methanamine chloride).

Compound 139 was synthesized by the reaction between macrocyclic triamine 138 and dimethoxy-Ar,Ar-di m e t hy 1 -methanamine in ethanol under reflux conditions (Equation 17) <1996JOC2020, 1997TL1911, 2001TL2735, 2004BCC174>. 

Methacrylic acid, methyl ester, see Methyl methacrylate Methaldehyde, see Formaldehyde Methanal, see Formaldehyde Methanamine, see Methylamine Methanecarbonitrile, see Acetonitrile Methanecarboxylic acid, see Acetic acid Methane dichloride, see Methylene chloride Methane tetrachloride, see Carbon tetrachloride Methanethiol, see Methyl mercaptan Methane trichloride, see Chloroform 6,9-Methano-2,4,3-benzodioxathiepin, see Endosnlfan sulfate... 

Fig. 9.9 Transformation of the phytoalexin brassinin (28) by (i) L. maculans virulent on canola to indole-3-carboxaldehyde (30) and (ii) L. maculans virulent on brown mustard to indolyl-3-methanamine (31)...

In the names of amines, the general use of suffixes and prefixes is not always observed. Normally, the suffix -amine would be added to the name of the parent hydride and engender names such as methanamine (CH3-NH2). Further substitution on the nitrogen atom would then be indicated by prefixes, leading to names that appear very cumbersome, such as A -methylmethanamine for (CH3)2NH and N,N-dimethylmethanamine for (CH3)3N. The traditional names of methylamine, di-methylamine and trimethylamine are much simpler. In these names, the term amine is not a suffix. It is, in fact, the name of the parent hydride, NH3, which now serves as the basis of substitutive names. Names such as diethylamine and tributylamine are representative of the preferred nomenclature. Diamines are named accordingly, as with ethane-1,2-diamine for H2N-CH2-CH2-NH2 and propane-1,3-diamine for H2N-[CH2]3-NH2. There are allowed alternatives for these last two compounds ethylenediamine and propane-1,3-diyldiamine. 

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