M79204
N -甲基吡咯烷
97%
别名:
1-Methylpyrrolidine, N-Methylpyrrolidine, N-Methyltetrahydropyrrole
质量水平
方案
97%
表单
liquid
沸点
80-81 °C (lit.)
密度
0.819 g/mL at 25 °C (lit.)
SMILES字符串
CN1CCCC1
InChI
1S/C5H11N/c1-6-4-2-3-5-6/h2-5H2,1H3
InChI key
AVFZOVWCLRSYKC-UHFFFAOYSA-N
应用
N-甲基吡咯烷可用作制备以下成分的起始材料：
N-甲基吡咯烷-硼氢化锌(ZBHNMP)——这是一种用于还原醛，酮，酰氯和酯的还原剂。ZBHNMP还用于将醛和酮还原胺化为相应的胺。
N-烷基-N-甲基-吡咯烷鎓双（三氟甲磺酰基）亚胺离子液体。
N-甲基吡咯烷-2-酮氢三溴化物可用作烯烃的叠氮化催化剂。
N-甲基吡咯烷-硼氢化锌(ZBHNMP)——这是一种用于还原醛，酮，酰氯和酯的还原剂。ZBHNMP还用于将醛和酮还原胺化为相应的胺。
N-烷基-N-甲基-吡咯烷鎓双（三氟甲磺酰基）亚胺离子液体。
N-甲基吡咯烷-2-酮氢三溴化物可用作烯烃的叠氮化催化剂。
警示用语：
Danger
危险分类
Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Flam. Liq. 2 - Skin Corr. 1A
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
-0.4 °F - closed cup
闪点(°C)
-18 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
N-methylpyrrolidine-2-one hydrotribromide: An efficient and new catalyst for the aziridination of alkenes using Chloramine-T under solvent free conditions
Jain SL, et al.
J. Mol. Catal. A: Chem., 256(1-2), 16-20 (2006)
Effect of the alkyl group on the synthesis and the electrochemical properties of N-alkyl-N-methyl-pyrrolidinium bis (trifluoromethanesulfonyl) imide ionic liquids
Appetecchi GB, et al.
Electrochimica Acta, 54(4), 1325-1332 (2009)
N-Methylpyrrolidine-zinc borohydride: As a new stable and efficient reducing agent in organic synthesis
Tajbakhsh M, et al.
Synthetic Communications, 33(2), 229-236 (2003)
Chafik Ghayor et al.
The Journal of biological chemistry, 286(27), 24458-24466 (2011-05-27)
Regulation of RANKL (receptor activator of nuclear factor κB ligand)-induced osteoclast differentiation is of current interest in the development of antiresorptive agents. Osteoclasts are multinucleated cells that play a crucial role in bone resorption. In this study, we investigated the
A R Salomon et al.
Biochemistry, 35(42), 13568-13578 (1996-10-22)
The 42-residues beta-(1-42) peptide is the major protein component of amyloid plaque cores in Alzheimer's disease. In aqueous solution at physiological pH, the synthetic beta-(1-42) peptide readily aggregates and precipitates as oligomeric beta-sheet structures, a process that occurs during amyloid
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