Cas no 69624-11-9 (3-Chloro-1H-pyrrole)
3-Chloro-1H-pyrrole Chemical and Physical Properties
Names and Identifiers
-
- 3-Chloro-1H-pyrrole
- 1H-Pyrrole, 3-chloro-
- 3-CHLOROPYRROLE
- 1H-Pyrrole,3-chloro
- AKOS006357513
- FT-0704505
- 69624-11-9
- SCHEMBL826848
- DTXSID70511395
- 1H-Pyrrole,3-chloro-
-
- Inchi: 1S/C4H4ClN/c5-4-1-2-6-3-4/h1-3,6H
- InChI Key: UUUOHRSINXUJKX-UHFFFAOYSA-N
- SMILES: ClC1C=CNC=1
Computed Properties
- Exact Mass: 101.00300
- Monoisotopic Mass: 101.0032268g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 6
- Rotatable Bond Count: 0
- Complexity: 46.8
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.3
- Topological Polar Surface Area: 15.8?2
Experimental Properties
- Density: 1.274
- Boiling Point: 181.225 °C at 760 mmHg
- Flash Point: 79.106 °C
- PSA: 15.79000
- LogP: 1.66810
3-Chloro-1H-pyrrole Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
3-Chloro-1H-pyrrole Customs Data
- HS CODE:2933990090
- Customs Data:
China Customs Code:
2933990090Overview:
2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
3-Chloro-1H-pyrrole Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | C375480-25mg |
3-Chloro-1H-pyrrole |
69624-11-9 | 25mg |
$201.00 | 2023-05-18 | ||
| TRC | C375480-250mg |
3-Chloro-1H-pyrrole |
69624-11-9 | 250mg |
$1303.00 | 2023-05-18 | ||
| TRC | C375480-500mg |
3-Chloro-1H-pyrrole |
69624-11-9 | 500mg |
$2291.00 | 2023-05-18 | ||
| TRC | C375480-750mg |
3-Chloro-1H-pyrrole |
69624-11-9 | 750mg |
$ 3000.00 | 2023-09-08 |
3-Chloro-1H-pyrrole Related Literature
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Xinhuan Wang,Shuangfei Cai,Cui Qi Analyst, 2017,142, 2500-2506
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Bo Wei,Zhenyu Liu,Chen Xie,Shu Yang,Wentao Tang,Aiwei Gu,Wing-Tak Wong,Ka-Leung Wong J. Mater. Chem. C, 2015,3, 12322-12327
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
Additional information on 3-Chloro-1H-pyrrole
Comprehensive Overview of 3-Chloro-1H-pyrrole (CAS No. 69624-11-9): Properties, Applications, and Industry Insights
3-Chloro-1H-pyrrole (CAS No. 69624-11-9) is a halogenated heterocyclic compound that has garnered significant attention in pharmaceutical and agrochemical research due to its versatile reactivity. As a chlorinated pyrrole derivative, it serves as a critical building block for synthesizing complex molecules, particularly in the development of bioactive compounds. The pyrrole ring structure is a hallmark of many natural products, making this compound a focal point for drug discovery and material science innovations.
Recent trends in organic synthesis highlight the growing demand for halogenated intermediates like 3-Chloro-1H-pyrrole. Researchers are actively exploring its utility in cross-coupling reactions, a topic frequently searched in academic databases and AI-driven platforms. The compound’s ability to undergo palladium-catalyzed transformations aligns with the industry’s shift toward sustainable catalysis, a hot topic in green chemistry forums. Notably, its electron-rich aromatic system enables diverse functionalizations, addressing queries about "modifying pyrrole cores for high-value applications."
From an industrial perspective, 69624-11-9 is pivotal in producing crop protection agents and pharmaceutical scaffolds. With increasing searches for "pyrrole-based fungicides" and "heterocyclic drug design," this compound’s role in agrochemical formulations and medicinal chemistry cannot be overstated. Its chloro-substitution enhances binding affinity to biological targets, a feature often discussed in structure-activity relationship (SAR) studies. Regulatory-compliant synthesis methods for 3-Chloro-1H-pyrrole are also a trending subtopic, reflecting concerns about process safety and environmental impact.
Analytical characterization of CAS 69624-11-9 typically involves GC-MS and NMR spectroscopy, techniques frequently queried by quality control professionals. The compound’s thermal stability and solubility profiles are critical for formulation scientists, as evidenced by search terms like "pyrrole derivative solubility in polar solvents." Furthermore, its crystallographic data is essential for computational chemists modeling molecular interactions, a niche yet growing area in AI-assisted drug discovery.
In material science, 3-Chloro-1H-pyrrole contributes to conductive polymers research, addressing searches for "organic electronic materials." Its incorporation into π-conjugated systems improves charge transport properties, a key focus for OLED and sensor technology developers. The compound’s electrophilic reactivity also makes it valuable for designing custom ligands in catalysis—a topic surging in metal-organic framework (MOF) research circles.
To optimize SEO visibility, this content integrates high-traffic keywords such as "pyrrole derivatives synthesis," "halogenated heterocycles applications," and "CAS 69624-11-9 suppliers," while maintaining technical rigor. By contextualizing 69624-11-9 within trending scientific discourse—from green synthesis to precision agriculture—this overview bridges industry gaps and enhances discoverability for researchers and procurement specialists alike.
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