294942
N,N-二环己基甲胺
97%
别名:
N-甲基二环己基胺
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关于此项目
线性分子式:
(C6H11)2NCH3
化学文摘社编号:
分子量:
195.34
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
231-453-4
Beilstein/REAXYS Number:
2074991
MDL number:
产品名称
N,N-二环己基甲胺, 97%
InChI key
GSCCALZHGUWNJW-UHFFFAOYSA-N
InChI
1S/C13H25N/c1-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13/h12-13H,2-11H2,1H3
SMILES string
CN(C1CCCCC1)C2CCCCC2
assay
97%
refractive index
n20/D 1.49 (lit.)
bp
265 °C (lit.)
density
0.912 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
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Application
N,N -二环己基甲胺的用途如下：
- 叔醇与有机铋 (V) 化合物 O 苯基化反应中的催化剂
- 1-（o-溴苯基）-2-甲基脯氨酸-2-烯-1-醇在钯催化下 5-内三角环化反应中的碱
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Sriram Kumar et al.
Nature communications, 11(1), 2960-2960 (2020-06-13)
Nucleic acid-based materials enable sub-nanometer precision in self-assembly for fields including biophysics, diagnostics, therapeutics, photonics, and nanofabrication. However, structural DNA nanotechnology has been limited to substantially hydrated media. Transfer to organic solvents commonly used in polymer and peptide synthesis results
Copper (II)-catalyzed O-phenylation of alcohols with organobismuth (V) reagents.
Sakurai N, et al.
ARKIVOC (Gainesville, FL, United States), 7, 254-264 (2007)
Heck-type reactions of allylic alcohols: Part IV:(2-Substituted)-1-indanones via 5-endo-trig cyclizations.
Zawisza AM, et al.
J. Mol. Catal. A: Chem., 283(1), 140-145 (2008)
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