3-Phenothiazone
Modify Date: 2025-08-25 18:47:23
3-Phenothiazone structure
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Common Name | 3-Phenothiazone | ||
|---|---|---|---|---|
| CAS Number | 581-30-6 | Molecular Weight | 213.25500 | |
| Density | 1.36g/cm3 | Boiling Point | 349.3ºC at 760 mmHg | |
| Molecular Formula | C12H7NOS | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 165ºC | |
| Name | phenothiazin-3-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.36g/cm3 |
|---|---|
| Boiling Point | 349.3ºC at 760 mmHg |
| Molecular Formula | C12H7NOS |
| Molecular Weight | 213.25500 |
| Flash Point | 165ºC |
| Exact Mass | 213.02500 |
| PSA | 58.20000 |
| LogP | 2.76130 |
| Index of Refraction | 1.72 |
| InChIKey | YKGCCFHSXQHWIG-UHFFFAOYSA-N |
| SMILES | O=c1ccc2nc3ccccc3sc-2c1 |
| Storage condition | 2-8°C |
| HS Code | 2934300000 |
|---|
| Precursor 9 | |
|---|---|
| DownStream 9 | |
CAS#:92-84-2
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CAS#:55847-59-1
CAS#:55847-65-9| HS Code | 2934300000 |
|---|---|
| Summary | 2934300000. other compounds containing in the structure a phenothiazine ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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|
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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|
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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|
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
|
|
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
|
|
Name: Small Molecule Inhibitors of FGF22-Mediated Excitatory Synaptogenesis & Epilepsy Meas...
Source: Broad Institute
Target: FGF22 human recombinant
External Id: 7012-04_Inhibitor_Dose_CherryPick_Activity
|
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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|
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
|
|
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
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| 3H-phenothiazine-3-one |
| phenothiazone |
| 3-Phenothiazone |
| phenothiazine-3-one |
| 3H-pheno-thiazinone |
| 3-phenothiazinone |