5-(4-chlorophenyl)-2-(2-propan-2-ylidenehydrazinyl)-1,3-thiazol-4-one
Modify Date: 2025-10-09 19:42:24
5-(4-chlorophenyl)-2-(2-propan-2-ylidenehydrazinyl)-1,3-thiazol-4-one structure
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Common Name | 5-(4-chlorophenyl)-2-(2-propan-2-ylidenehydrazinyl)-1,3-thiazol-4-one | ||
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| CAS Number | 55073-95-5 | Molecular Weight | 281.76100 | |
| Density | 1.39g/cm3 | Boiling Point | 415.8ºC at 760 mmHg | |
| Molecular Formula | C12H12ClN3OS | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 205.3ºC | |
| Name | 5-(4-chlorophenyl)-2-(2-propan-2-ylidenehydrazinyl)-1,3-thiazol-4-one |
|---|
| Density | 1.39g/cm3 |
|---|---|
| Boiling Point | 415.8ºC at 760 mmHg |
| Molecular Formula | C12H12ClN3OS |
| Molecular Weight | 281.76100 |
| Flash Point | 205.3ºC |
| Exact Mass | 281.03900 |
| PSA | 79.12000 |
| LogP | 3.32470 |
| Index of Refraction | 1.661 |
| InChIKey | KRIHEFMSOJMNSZ-UHFFFAOYSA-N |
| SMILES | CC(C)=NN=C1NC(=O)C(c2ccc(Cl)cc2)S1 |
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5-(4-chlorophen... CAS#:55073-95-5 |
| Literature: Reeve,W.; Barron,E.R. Journal of Organic Chemistry, 1975 , vol. 40, p. 1917 - 1920 |
| Precursor 2 | |
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| DownStream 0 | |
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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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
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|
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
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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: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_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
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