M72609
N-甲基哌啶
99%
别名:
1-甲基哌啶
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关于此项目
经验公式（希尔记法）:
C6H13N
化学文摘社编号:
分子量:
99.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-959-9
Beilstein/REAXYS Number:
1073
MDL number:
产品名称
N-甲基哌啶, 99%
InChI key
PAMIQIKDUOTOBW-UHFFFAOYSA-N
InChI
1S/C6H13N/c1-7-5-3-2-4-6-7/h2-6H2,1H3
SMILES string
CN1CCCCC1
assay
99%
refractive index
n20/D 1.4378 (lit.)
bp
106-107 °C (lit.)
density
0.816 g/mL at 25 °C (lit.)
Quality Level
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Application
反应物用于：
用于合成以下物质的反应物：
- sp3 C-H 键通过钌 (II) 催化剂与环胺 C (3) 烷基化反应活化
- Z-肉桂酸的一锅法合成
用于合成以下物质的反应物：
- 不对称尿素酶
- 抗菌咪唑、吡咯烷和哌啶盐
- 通过钯催化的有机锡硫代酯偶联反应，得到角化酶A的C1-C16片段
- 胰岛素样生长因子-1 受体和 ErbB 家族受体激酶的多靶点抑制剂
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
37.4 °F - closed cup
flash_point_c
3 °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
Xuenan Li et al.
Journal of food science, 85(9), 2754-2761 (2020-08-15)
N,N-dimethylpiperidinium (mepiquat) is a new process-induced compound formed from natural constituents during the cooking process. Mepiquat was first found in coffee and cereal products, but its formation mechanism in coffee is still unclear. In the current study, Arabica and Robusta
Oscar B Torres et al.
Analytical and bioanalytical chemistry, 410(16), 3885-3903 (2018-04-21)
We describe for the first time a method that utilizes microscale thermophoresis (MST) technology to determine polyclonal antibody affinities to small molecules. Using a novel type of heterologous MST, we have accurately measured a solution-based binding affinity of serum antibodies
Bing Yu et al.
Bioorganic & medicinal chemistry letters, 22(1), 110-114 (2011-12-16)
We report herein the design and synthesis of novel 4-aminoquinazoline derivatives based on the inhibitors of VEGFR-2 tyrosine kinases. The VEGFR-2 inhibitory activities of these newly synthesized compounds were also evaluated and compared with that of ZD6474. We found that
A Kolocouris et al.
The Journal of organic chemistry, 66(15), 4989-4997 (2001-07-21)
When a 1-adamantyl or a 2-adamantyl substituent is introduced at the 2-position in N-methylpiperidine, four different chair conformations are possible. Experimental observation using dynamic NMR spectroscopy and molecular mechanics calculations agree that the chair conformation with an equatorial adamantyl group
[The mechanism of reverse inhibition of cholinesterases by thionphosphonates].
N N Kovalev et al.
Izvestiia Akademii nauk SSSR. Seriia biologicheskaia, (6)(6), 926-929 (1988-11-01)
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