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Merck
CN

M79204

N -甲基吡咯烷

97%

别名:

1-Methylpyrrolidine, N-Methylpyrrolidine, N-Methyltetrahydropyrrole

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关于此项目

经验公式(希尔记法):
C5H11N
化学文摘社编号:
分子量:
85.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-438-5
Beilstein/REAXYS Number:
102445
MDL number:
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产品名称

N -甲基吡咯烷, 97%

InChI

1S/C5H11N/c1-6-4-2-3-5-6/h2-5H2,1H3

InChI key

AVFZOVWCLRSYKC-UHFFFAOYSA-N

SMILES string

CN1CCCC1

assay

97%

form

liquid

bp

80-81 °C (lit.)

density

0.819 g/mL at 25 °C (lit.)

Quality Level

Application

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。

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Flam. Liq. 2 - Skin Corr. 1A

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-0.4 °F - closed cup

flash_point_c

-18 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
Reductive amination of aldehydes and ketones to their corresponding amines with N-methylpyrrolidine zinc borohydride
Alinezhad H, et al.
Tetrahedron Letters, 50(6), 659-661 (2009)
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

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