Factory Supply High Purity 99% 2,5-Dimethyl-1H-pyrrole 625-84-3 On Stock
- Molecular Formula:C6H9N
- Molecular Weight:95.1442
- Appearance/Colour:clear yellow to orange-brown liquid
- Vapor Pressure:2.5mmHg at 25°C
- Melting Point:6.5oC
- Refractive Index:n20/D 1.505(lit.)
- Boiling Point:165.1 °C at 760 mmHg
- PKA:18.46±0.50(Predicted)
- Flash Point:54.4 °C
- PSA：15.79000
- Density:0.948 g/cm3
- LogP:1.63150
2,5-Dimethyl-1H-pyrrole(Cas 625-84-3) Usage
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Chemical Properties
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clear yellow to orange-brown liquid
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Synthesis Reference(s)
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Synthetic Communications, 18, p. 167, 1988 DOI: 10.1080/00397918808077341Synthesis, p. 1585, 2000 DOI: 10.1055/s-2000-7618
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Safety Profile
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When heated to decomposition emits toxic fumes of NOx
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InChI:InChI=1/C6H9N/c1-5-3-4-6(2)7-5/h3-4,7H,1-2H3
625-84-3 Relevant articles
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Whipple et al.
, p. 26,29 (1963)
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An improved method for the preparation of N-unsubstituted 1,4,5,6-tetrahydrocyclopenta[b]pyrroles: Synthesis of an azaprostacyclin analogue and its 7-cyano derivative
Rousseau, Brigitte,Nydegger, Fredy,Gossauer, Albert,Bennua-Skalmowski, Baerbel,Vorbrueggen, Helmut
, p. 1336 - 1340 (1996)
Paal-Knorr cyclization of 2-acetonylcycl...
An expeditious and highly efficient synthesis of substituted pyrroles using a low melting deep eutectic mixture
Alvi, Shakeel,Ali, Rashid
, p. 9732 - 9745 (2021/12/01)
An expeditious green method for the synt...
Synthesis of gamma dicarbonyl and pyrrole compounds
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Page/Page column 19, (2019/03/01)
The present invention discloses processe...
Thermal Behavior Analysis of Two Synthesized Flavor Precursors of N-alkylpyrrole Derivatives
Ai, Lvye,Liu, Mengzhen,Ji, Xiaoming,Lai, Miao,Zhao, Mingqin,Ren, Tianbao
, p. 2389 - 2397 (2019/08/01)
To expand the library of pyrrole-contain...
Acceptorless Dehydrogenative Coupling Using Ammonia: Direct Synthesis of N-Heteroaromatics from Diols Catalyzed by Ruthenium
Daw, Prosenjit,Ben-David, Yehoshoa,Milstein, David
supporting information, p. 11931 - 11934 (2018/09/27)
The synthesis of N-heteroaromatic compou...
625-84-3 Process route
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- 143-33-9,25596-52-5
sodium cyanide
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- 78133-60-5
N-(2,5-dimethylpyrrol-1-yl)pyridinium iodide
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- 625-84-3
2,5-Dimethylpyrrole
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- 100-48-1
pyridine-4-carbonitrile
Conditions
| Conditions |
Yield |
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In water; at 100 ℃; for 0.5h;
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33% |
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- 2935-44-6
hexane-2,5-diol
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- 822-64-0
2,5-dimethyl-1-pyrroline
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- 625-84-3
2,5-Dimethylpyrrole
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- 5044-19-9
1-ethyl-2,5-dimethyl-1H-pyrrole
Conditions
| Conditions |
Yield |
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With carbonylchlorohydrido(4,5-bis((diisopropylphosphino)methyl)acridine)ruthenium(II); ammonia; In toluene; at 150 ℃; for 24h; under 5250.53 Torr; Inert atmosphere; Glovebox;
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71 %Spectr.
20 %Spectr.
7 %Spectr. |
625-84-3 Upstream products
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2199-52-2
2,5-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester
625-84-3 Downstream products
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6312-14-7
2-[2-(2,5-dimethyl-pyrrol-1-yl)-ethyl]-pyridine
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1500-94-3
3-acetyl-2,5-dimethylpyrrole
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5435-88-1
3,4-bis-dimethylaminomethyl-2,5-dimethyl-pyrrole
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2405-06-3
3-chloro-2,6-dimethylpyridine
