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M78801

Sigma-Aldrich

N-Methylpyrrole

99%

Sinónimos:

1-Methyl-1H-pyrrole, N-Methylpyrrole

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About This Item

Fórmula empírica (notación de Hill):
C5H7N
Número de CAS:
96-54-8
Peso molecular:
81.12
Beilstein/REAXYS Number:
104181
EC Number:
202-513-7
MDL number:
MFCD00005345
UNSPSC Code:
12352100
PubChem Substance ID:
24897193
NACRES:
NA.22

vapor density

2.8 (vs air)

vapor pressure

15 mmHg ( 20.2 °C)

assay

99%

form

liquid

expl. lim.

6 %

bp

112-113 °C (lit.)

mp

−57 °C (lit.)

density

0.914 g/mL at 25 °C (lit.)

SMILES string

Cn1cccc1

InChI

1S/C5H7N/c1-6-4-2-3-5-6/h2-5H,1H3

Inchi Key

OXHNLMTVIGZXSG-UHFFFAOYSA-N

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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

60.8 °F - closed cup

flash_point_c

16 °C - closed cup

ppe

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

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Pyrrole reagent grade, 98%

Sigma-Aldrich

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Pyrrole

N-Boc-pyrrole 98%

Sigma-Aldrich

425834

N-Boc-pyrrole

2,4-Dimethylpyrrole 97%

Sigma-Aldrich

390836

2,4-Dimethylpyrrole

N,N-Diisopropylaniline 97%

Sigma-Aldrich

436860

N,N-Diisopropylaniline

Giovanni Piani et al.
The journal of physical chemistry. A, 113(52), 14554-14558 (2009-10-16)
We investigated the reaction dynamics of N-methylpyrrole (NMP) along the N-CH3 coordinate, upon excitation energies below 6.4 eV. Ours and previous experiments show clearly the existence of different reaction channels leading to slow and fast fragment production whose relative efficiency
Gengo Kashiwazaki et al.
Bioorganic & medicinal chemistry, 17(3), 1393-1397 (2009-01-07)
We designed and synthesized alkylating conjugates 5-7 and their partner N-methylpyrrole-N-methylimidazole (PI) polyamides 8, 9. The DNA alkylating activities of conjugates 5-7 were evaluated by high-resolution denaturing polyacrylamide gel electrophoresis with a 219 base pair (bp) DNA fragment containing the
Mingyu Niu et al.
Rapid communications in mass spectrometry : RCM, 20(7), 1077-1081 (2006-02-25)
Different negative fragmentations of synthesized polyamides containing N-methylpyrrole and N-methylimidazole were analyzed by electrospray ionization tandem mass spectrometry with low-energy collision-induced dissociation. An interesting rearrangement derived from amino catalysis of N-methylimidazole was observed. The observation is useful for the study
Shigeki Nishijima et al.
Bioorganic & medicinal chemistry, 18(2), 978-983 (2009-12-22)
In order to investigate the influence of molecular size and pyrrole (Py)/imidazole (Im) content on the cell permeability of Py-Im-polyamide-fluorescein conjugates we systematically designed the Py-polyamides and Im-polyamides. Flow cytometric analysis revealed that Py-polyamides, even those with large molecular size
Jiang Zhou et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(4), 1157-1162 (2004-12-30)
Electrospray ionization mass spectrometry (ESI-MS) was used to investigate noncovalent complexes formed between four novel polyamides containing N-methylpyrrole (Py) and N-methylimidazole (Im), and human telomeric DNA. Of the four polyamides investigated, PyPyPygammaImImImbetaDp (3) had the highest binding affinity towards the
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