P73404
吡咯-2-甲醛
98%
别名:
2-甲酰基吡咯
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关于此项目
经验公式（希尔记法）:
C5H5NO
化学文摘社编号:
分子量:
95.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-705-5
Beilstein/REAXYS Number:
105745
MDL number:
Assay:
98%
Form:
crystals
InChI
1S/C5H5NO/c7-4-5-2-1-3-6-5/h1-4,6H
InChI key
ZSKGQVFRTSEPJT-UHFFFAOYSA-N
SMILES string
[H]C(=O)c1ccc[nH]1
assay
98%
form
crystals
bp
217-219 °C (lit.)
mp
43-46 °C (lit.)
storage temp.
2-8°C
Quality Level
General description
2-吡咯甲醛是一种杂环合成砌块，由2位连接甲酰基的吡咯环组成，用于生产各种生物活性物质。 高度官能化的2-吡咯甲醛已用作中间体制备吡咯低聚物大环。
Application
- 用于检测铜绿假单胞菌的基于嘧啶的荧光有机纳米粒子探针：这项研究使用吡咯-2-甲醛开发了一种基于嘧啶的荧光纳米粒子探针，用于检测铜绿假单胞菌，增强了微生物学的诊断能力（Kaur G等人，2015年）。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Investigation of optical and electrical properties of Pyrrole-2- carboxyldehyde (PCL) in PVA polymer matrix
Rana, Meenakshi and Devlal, et al.
Materials Today: Proceedings, 49, 3279-3282 (2022)
Z H Chohan et al.
Chemical & pharmaceutical bulletin, 40(9), 2555-2556 (1992-09-01)
A new Schiff-base ligand N-(2'-pyrrylmethylidene)2-aminopyrimidine derived from the reaction of 2-amino pyrimidine and pyrrol-2-carboxaldehyde and its nickel(II), copper(II) and zinc(II) complexes have been synthesised and characterised on the basis of elemental analysis, molar conductance, infrared, electronic and proton nuclear magnetic
Huajian Zhu et al.
Organic letters, 13(10), 2792-2794 (2011-04-23)
A new synthetic protocol for efficient and regiospecifc assembly of indolizines and pyrido[1,2-a]indoles by coupling of substituted methyl bromides and alkynes with corresponding pyrrole-2-carboxaldehyde and 1H-indole-2-carboxaldehyde has been developed. Additionally, a possible mechanism for the reaction is proposed.
Takumi Ishizuka et al.
Chemical communications (Cambridge, England), 48(88), 10835-10837 (2012-10-04)
Toward new biotechnology by genetic alphabet expansion, we developed an efficient site-specific labeling method for large RNA molecules. The combination of unnatural base pair transcription and post-transcriptional modification by click chemistry enables simple RNA labeling with a wide variety of
Corey A Rice et al.
The Journal of chemical physics, 126(13), 134313-134313 (2007-04-14)
Intermolecular interactions relevant for antiparallel beta-sheet formation between peptide strands are studied by Fourier transform infrared spectroscopy of the low temperature, vacuum-isolated model compound pyrrole-2-carboxaldehyde and its dimer in the N-H and C=O stretching range. Comparison to quantum chemical predictions
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