ethyl 5-(methoxy-phenoxy-methyl)thiadiazole-4-carboxylate
Modify Date: 2025-09-22 11:54:29
ethyl 5-(methoxy-phenoxy-methyl)thiadiazole-4-carboxylate structure
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Common Name | ethyl 5-(methoxy-phenoxy-methyl)thiadiazole-4-carboxylate | ||
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| CAS Number | 4609-55-6 | Molecular Weight | 294.32600 | |
| Density | 1.29g/cm3 | Boiling Point | 428.6ºC at 760 mmHg | |
| Molecular Formula | C13H14N2O4S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 213ºC | |
| Name | ethyl 5-[methoxy(phenoxy)methyl]thiadiazole-4-carboxylate |
|---|---|
| Synonym | More Synonyms |
| Density | 1.29g/cm3 |
|---|---|
| Boiling Point | 428.6ºC at 760 mmHg |
| Molecular Formula | C13H14N2O4S |
| Molecular Weight | 294.32600 |
| Flash Point | 213ºC |
| Exact Mass | 294.06700 |
| PSA | 98.78000 |
| LogP | 2.43880 |
| Index of Refraction | 1.569 |
| InChIKey | QEQFAVWEQCQODI-UHFFFAOYSA-N |
| SMILES | CCOC(=O)c1nnsc1C(OC)Oc1ccccc1 |
| HS Code | 2934999090 |
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~%
ethyl 5-(methox... CAS#:4609-55-6 |
| Literature: Looker,J.H.; Wilson,L.W. Journal of Heterocyclic Chemistry, 1965 , vol. 2, p. 348 - 354 |
|
~%
ethyl 5-(methox... CAS#:4609-55-6 |
| Literature: Looker,J.H.; Wilson,L.W. Journal of Heterocyclic Chemistry, 1965 , vol. 2, p. 348 - 354 |
|
~%
ethyl 5-(methox... CAS#:4609-55-6 |
| Literature: Looker,J.H.; Wilson,L.W. Journal of Heterocyclic Chemistry, 1965 , vol. 2, p. 348 - 354 |
![5-(bromo-phenoxy-methyl)-[1,2,3]thiadiazole-4-carboxylic acid ethyl ester structure](https://image.chemsrc.com/caspic/061/4609-56-7.png)
CAS#:4609-58-9| HS Code | 2934999090 |
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| 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: 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: High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS1149-MLP
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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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