359327
N-己基甲胺
96%
别名:
N-甲基己胺
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关于此项目
线性分子式:
CH3NH(CH2)5CH3
化学文摘社编号:
分子量:
115.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
252-410-6
Beilstein/REAXYS Number:
1731685
MDL number:
Assay:
96%
Form:
liquid
InChI key
XJINZNWPEQMMBV-UHFFFAOYSA-N
InChI
1S/C7H17N/c1-3-4-5-6-7-8-2/h8H,3-7H2,1-2H3
SMILES string
CCCCCCNC
assay
96%
form
liquid
refractive index
n20/D 1.416 (lit.)
bp
140-142 °C (lit.)
density
0.76 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
General description
N-Hexylmethylamine is an acyclic secondary amine. Ruthenium-catalyzed reaction of N-hexylmethylamine with styrene has been reported. Transition metal-catalyzed intermolecular hydroamination of N-hexylmethylamine with 2-vinylnaphthalene has been reported.
Application
N-Hexylmethylamine may be used in the synthesis of dialkyldithiocarbamato cadmium complexes Cd[S2CNRR′]2.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
87.8 °F - closed cup
flash_point_c
31 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
The synthesis of SiO2@ CdS nanocomposites using single-molecule precursors.
Monteiro OC, et al.
Chemistry of Materials, 14(7), 2900-2904 (2002)
Masaru Utsunomiya et al.
Journal of the American Chemical Society, 125(47), 14286-14287 (2003-11-20)
A transition metal-catalyzed intermolecular hydroamination of vinylarenes with alkylamines is reported. The combination of Pd(O2CCF3)4, DPPF, and TfOH was the most effective catalyst of those tested. Control experiments without palladium, acid, or ligand all occurred in low yield. The reaction
Masaru Utsunomiya et al.
Journal of the American Chemical Society, 126(9), 2702-2703 (2004-03-05)
A ruthenium-catalyzed intermolecular, anti-Markovnikov hydroamination of vinylarenes with secondary aliphatic and benzylic amines is reported. The combination of Ru(cod)(2-methylallyl)2, 1,5-bis(diphenylphosphino)pentane, and triflic acid was the most effective catalyst of those tested. Control reactions conducted without ligand or acid did not
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