Cas no 18992-86-4 (9H-Carbazol-1-amine)
9H-Carbazol-1-amine Chemical and Physical Properties
Names and Identifiers
-
- 9H-Carbazol-1-amine
- 1-AMINOCARBAZOLE
- SCHEMBL194195
- aminocarbazole
- 9H-Carbazolamine
- AMY24317
- 38886-78-1
- A924533
- 9H-Carbazol-1-ylamine
- MFCD18450159
- 18992-86-4
- SY272796
- DTXSID60940519
- AKOS006239264
- DB-108351
- BS-53401
-
- MDL: MFCD18450159
- Inchi: 1S/C12H10N2/c13-10-6-3-5-9-8-4-1-2-7-11(8)14-12(9)10/h1-7,14H,13H2
- InChI Key: YJKJAYFKPIUBAW-UHFFFAOYSA-N
- SMILES: N1C2C=CC=CC=2C2C=CC=C(C1=2)N
Computed Properties
- Exact Mass: 181.07667
- Monoisotopic Mass: 182.084398
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 14
- Rotatable Bond Count: 0
- Complexity: 216
- 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: 3
- Topological Polar Surface Area: 41.8
Experimental Properties
- Density: 1.317
- Boiling Point: 440.8°Cat760mmHg
- Flash Point: 250.6°C
- Refractive Index: 1.827
- PSA: 38.91
9H-Carbazol-1-amine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A449038070-250mg |
9H-Carbazol-1-amine |
18992-86-4 | 95% | 250mg |
$175.96 | 2023-09-02 | |
| Alichem | A449038070-1g |
9H-Carbazol-1-amine |
18992-86-4 | 95% | 1g |
$405.72 | 2023-09-02 | |
| Alichem | A449038070-5g |
9H-Carbazol-1-amine |
18992-86-4 | 95% | 5g |
$1367.40 | 2023-09-02 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBGWZX064-100mg |
9H-carbazol-1-amine |
18992-86-4 | 95% | 100mg |
¥713.0 | 2024-04-23 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBGWZX064-250mg |
9H-carbazol-1-amine |
18992-86-4 | 95% | 250mg |
¥951.0 | 2024-04-23 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBGWZX064-500mg |
9H-carbazol-1-amine |
18992-86-4 | 95% | 500mg |
¥1590.0 | 2024-04-23 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBGWZX064-1g |
9H-carbazol-1-amine |
18992-86-4 | 95% | 1g |
¥2382.0 | 2024-04-23 | |
| Aaron | AR002EUI-10g |
9H-carbazol-1-amine |
18992-86-4 | 98% | 10g |
$2341.00 | 2025-02-12 | |
| eNovation Chemicals LLC | Y0999220-1g |
9H-Carbazol-1-amine |
18992-86-4 | 95% | 1g |
$300 | 2025-02-18 | |
| A2B Chem LLC | AB11454-100mg |
9H-Carbazol-1-amine |
18992-86-4 | 95% | 100mg |
$62.00 | 2024-04-20 |
9H-Carbazol-1-amine Suppliers
9H-Carbazol-1-amine Related Literature
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L. Di Michele,D. Fiocco,F. Varrato,E. Eiser,G. Foffi Soft Matter, 2014,10, 3633-3648
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Felix Witte,Philipp Rietsch,Nithiya Nirmalananthan-Budau,Florian Weigert,Jan P. G?tze,Ute Resch-Genger,Siegfried Eigler,Beate Paulus Phys. Chem. Chem. Phys., 2021,23, 17521-17529
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Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
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Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre Albrecht Chem. Commun., 2001, 1976-1977
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Xin Fu,Qing-rong Liang,Rong-guang Luo,Yan-shu Li,Xiao-ping Xiao,Lu-lu Yu,Wen-zhe Shan,Guang-qin Fan J. Mater. Chem. B, 2019,7, 3088-3099
Additional information on 9H-Carbazol-1-amine
Recent Advances in the Study of 9H-Carbazol-1-amine (CAS: 18992-86-4) in Chemical Biology and Pharmaceutical Research
9H-Carbazol-1-amine (CAS: 18992-86-4) is a heterocyclic compound that has garnered significant attention in recent years due to its potential applications in medicinal chemistry and drug development. This compound, characterized by its carbazole scaffold, has been the subject of numerous studies aimed at exploring its biological activities, synthetic pathways, and therapeutic potential. The carbazole core is known for its diverse pharmacological properties, including antitumor, antimicrobial, and anti-inflammatory effects, making 9H-Carbazol-1-amine a promising candidate for further investigation.
Recent research has focused on the synthesis and modification of 9H-Carbazol-1-amine to enhance its bioactivity and pharmacokinetic properties. A study published in the Journal of Medicinal Chemistry (2023) demonstrated that introducing specific substituents at the 1-amino position could significantly improve the compound's binding affinity to target proteins, such as kinases and G-protein-coupled receptors (GPCRs). These modifications have led to the development of novel derivatives with enhanced selectivity and potency, paving the way for their potential use in treating various diseases, including cancer and neurodegenerative disorders.
In addition to its therapeutic potential, 9H-Carbazol-1-amine has also been investigated for its role in chemical biology. A recent study in ACS Chemical Biology (2024) highlighted its utility as a fluorescent probe for imaging cellular processes. The compound's inherent fluorescence properties, combined with its ability to penetrate cell membranes, make it an attractive tool for real-time monitoring of intracellular events. This application could provide valuable insights into disease mechanisms and facilitate the development of targeted therapies.
Another area of interest is the environmental and toxicological profile of 9H-Carbazol-1-amine. A 2023 study in Environmental Science & Technology evaluated the compound's stability and degradation pathways under various environmental conditions. The findings suggested that while 9H-Carbazol-1-amine is relatively stable in aqueous solutions, it can undergo photodegradation in the presence of sunlight, leading to the formation of less toxic byproducts. This information is crucial for assessing the environmental impact of its widespread use in pharmaceutical and industrial applications.
In conclusion, 9H-Carbazol-1-amine (CAS: 18992-86-4) represents a versatile and promising compound in the fields of chemical biology and pharmaceutical research. Its unique structural features, combined with its diverse biological activities, make it a valuable candidate for further exploration. Ongoing studies are expected to uncover new applications and optimize its properties for clinical use, ultimately contributing to advancements in drug discovery and development.
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