Detail of "14489-75-9"

CAS Number:
14489-75-9
Name:
1-Naphthalenemethanamine,N-methyl-
Superlist Name:
1-Methyl-aminomethyl naphthalene
Molecular Structure:
Formula:
C₁₂H₁₃N
Molecular Weight:
171.24
Synonyms:
N-Methyl-1-naphthalenemethylamine;N-Methyl-N-[(naphthalen-1-yl)methyl]amine;NSC 129392;[(Naphthalen-1-yl)methyl]methylamine;N-(Naphthalen-1-yl-methyl)-N-methylamine;1-Naphthalenemethylamine,N-methyl- (6CI,8CI);Methyl(1-naphthylmethyl)amine;
EINECS:
238-497-3
Density:
1.036 g/cm³
Boiling Point:
287.873 °C at 760 mmHg
Flash Point:
146.629 °C
Hazard Symbols:
Xi
Risk Codes:
36/37/38
Safety:
26-36/37/39 Details

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(1-Naphthylmethyl) amine derivatives: (1-Naphthylmethyl) amine derivatives. Berney, Daniel (Sandoz-Patent-G.m.b.H., Switz.). Ger. Offen. DE 2716943 17 Nov 1977, 27 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07C087-29. PRIORITY: CH 76-5335 28 Apr 1976. DOCUMENT TYPE: Patent CA Section: 26 (Condensed Aromatic Compounds) Section cross-reference(s): 63 The title compds. There are some commonly used reagents like 14489-75-9 in this article. I (R1 = H, alkyl; R2 = cycloalkylalkyl, alkyl, alkenyl, alkynyl; R3 = H, alkyl; R4-7 = H, halo, CF3, HO, NO2, alkoxy), useful as antimycotics (dosage ranges given), were prepd. Thus, treating II with PhCH:CHCH2Cl in DMF contg.In this study，14489-75-9 is also used. Na2CO3 gave I (R1, R3-7 = H; R2 = Me). ..

A Simple Method for Obtaining Terbinafine Hydrochloride: A Simple Method for Obtaining Terbinafine Hydrochloride. Kazakov, P. V.; Golosov, S. N.Some commonly used reagents like 14489-75-9 is used in this experiment. 14489-75-9 is the cas registry number. This chemical is also mentioned in this article. (State Research Institute of Organic Chemistry and Technology, Moscow, Russia). Pharmaceutical Chemistry Journal (Translation of Khimiko-Farmatsevticheskii Zhurnal), 38(4), 206-208 (English) 2004 Kluwer Academic/Consultants Bureau. CODEN: PCJOAU. ISSN: 0091-150X. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Terbinafine hydrochloride (I) was prepd. in 91% yield by alkylation of N-methyl-1-naphthalenemethanamine with (E)-1-chloro-6,6-dimethyl-2-hepten-4-yne in the presence of 15% aq. NaOH, followed by addn. of HCl. ..