2-thiophen-2-yl-quinoline-4-carboxylic acid
Modify Date: 2025-09-24 10:13:23
2-thiophen-2-yl-quinoline-4-carboxylic acid structure
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Common Name | 2-thiophen-2-yl-quinoline-4-carboxylic acid | ||
|---|---|---|---|---|
| CAS Number | 31792-47-9 | Molecular Weight | 255.29200 | |
| Density | N/A | Boiling Point | 458.1ºC at 760mmHg | |
| Molecular Formula | C14H9NO2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 230.8ºC | |
| Name | 2-thiophen-2-ylquinoline-4-carboxylic acid |
|---|---|
| Synonym | More Synonyms |
| Boiling Point | 458.1ºC at 760mmHg |
|---|---|
| Molecular Formula | C14H9NO2S |
| Molecular Weight | 255.29200 |
| Flash Point | 230.8ºC |
| Exact Mass | 255.03500 |
| PSA | 78.43000 |
| LogP | 3.66150 |
| Index of Refraction | 1.712 |
| InChIKey | YDZHUFHFHQWQQB-UHFFFAOYSA-N |
| SMILES | O=C(O)c1cc(-c2cccs2)nc2ccccc12 |
| Hazard Codes | Xi: Irritant; |
|---|---|
| HS Code | 2934999090 |
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~80%
2-thiophen-2-yl... CAS#:31792-47-9 |
| Literature: Mitachi, Katsuhiko; Salinas, Yandira G.; Connelly, Michele; Jensen, Nicholas; Ling, Taotao; Rivas, Fatima Bioorganic and Medicinal Chemistry Letters, 2012 , vol. 22, # 14 p. 4536 - 4539 |
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~92%
2-thiophen-2-yl... CAS#:31792-47-9 |
| Literature: Belen'kaya, R. S.; Boreko, E. I.; Zemtsova, M. N.; Kalinina, M. I.; Timofeeva, M. M.; et al. Pharmaceutical Chemistry Journal, 1981 , vol. 15, # 3 p. 171 - 176 Khimiko-Farmatsevticheskii Zhurnal, 1981 , vol. 15, # 3 p. 29 - 35 |
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~%
2-thiophen-2-yl... CAS#:31792-47-9 |
| Literature: Pharmaceutical Chemistry Journal, , vol. 15, # 3 p. 171 - 176 Khimiko-Farmatsevticheskii Zhurnal, , vol. 15, # 3 p. 29 - 35 |
|
~%
2-thiophen-2-yl... CAS#:31792-47-9 |
| Literature: Pharmaceutical Chemistry Journal, , vol. 15, # 3 p. 171 - 176 Khimiko-Farmatsevticheskii Zhurnal, , vol. 15, # 3 p. 29 - 35 |
![3-hydroxy-3-[2-oxo-2-(thiophen-2-yl)ethyl]-1,3-dihydro-2H-indol-2-one structure](https://image.chemsrc.com/caspic/456/78660-85-2.png)
| HS Code | 2934999090 |
|---|---|
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Name: qHTS screening for TAG (triacylglycerol) accumulators in algae
Source: 11812
Target: N/A
External Id: FATTTLab-Algae-Lipid
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Name: Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: HCMV UL50
External Id: HMS1262
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Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
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Name: Cell-based high throughput primary assay to identify activators of GPR151
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id: GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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Name: A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: Chain A, Poliovirus Polymerase With Gtp
External Id: HMS750
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Name: Antimalarial activity against chloroquine-resistant Plasmodium falciparum 3D7 incubat...
Source: ChEMBL
Target: Plasmodium falciparum
External Id: CHEMBL2049755
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Name: Antimalarial activity against chloroquine-resistant Plasmodium falciparum 3D7 incubat...
Source: ChEMBL
Target: Plasmodium falciparum
External Id: CHEMBL2049756
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Name: Cytotoxicity against human BJ cells after 72 hrs by resazurin dye based CellTiterGlo ...
Source: ChEMBL
Target: BJ
External Id: CHEMBL2049759
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Name: Cytotoxicity against human HEK293 cells after 72 hrs by resazurin dye based CellTiter...
Source: ChEMBL
Target: HEK293
External Id: CHEMBL2049760
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Name: Cytotoxicity against human HepG2 cells after 72 hrs by resazurin dye based CellTiterG...
Source: ChEMBL
Target: HepG2
External Id: CHEMBL2049757
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| 2-(2-thienyl)quinoline-4-carboxylic acid |
| MFCD00178258 |
| 2-(2-Thienyl)-4-quinolinecarboxylic acid |
| 2-thien-2-ylquinoline-4-carboxylic acid |
| 2-[2-Thienyl]cinchoninic acid |
| 2-[2]Thienyl-chinolin-4-carbonsaeure |
| 2-(thiophen-2-yl)quinoline-4-carboxylic acid |